Cleared Traditional

K050230 - TURBO TEMP TRIO

K050230 is an FDA 510(k) clearance for TURBO TEMP TRIO, manufactured by Cardinal Health, Alaris Products. The device is a Class 2 General Hospital device with product code FLL cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K050230 · Cardinal Health, Alaris Products · General Hospital
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Optimized for regulatory review, auditing and printing
Feb 2005
Decision
15d
Days
Class 2
Risk

K050230 is an FDA 510(k) clearance for the TURBO TEMP TRIO. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by Cardinal Health, Alaris Products (San Diego, US). The FDA issued a Cleared decision on February 16, 2005 after a review of 15 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.2910 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Cardinal Health, Alaris Products devices

FDA 510(k) Submission Details - K050230

510(k) Number K050230 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 2005
Decision Date February 16, 2005
Days to Decision 15 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
114d faster than avg
Panel avg: 129d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

FLL Device Classification - Class 2, Special Controls

Product Code FLL Continuous Measurement Thermometer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.2910
Definition A Continuous Measurement Thermometer Is A Clinical Electronic Thermometer Indicated To Measure The Body Or Skin Temperature Of A Person Continuously Or In Specified Intervals. Under This Regulation, This Product Code Represents Non-exempt Devices. For More Information, See 90 Fr 25889, Available At Https://www.govinfo.gov/content/pkg/fr-2025-06-18/pdf/2025-11207.pdf.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Consultant

Entela, Inc.
NEIL E DEVINE

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - FLL Continuous Measurement Thermometer

All 646
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K050230.
TEMPTOUCH DERMAL THERMOMETER
K050137 · Xilas Medical, Inc. · Mar 2005
DIGITAL FOREHEAD THERMOMETER, MODEL FS-100
K043331 · Hubdic Co., Ltd. · Mar 2005
5 SEC DIGITAL CLINICAL THERMOMETER, MODELS ST8630X, ST8640X, ST8730X, ST8740X, ST8930X, ST8940X, ST8030X, ST8040X.
K050303 · Mesure Technology Co., Ltd. · Feb 2005
CLINICAL ELECTRONIC THERMOMETER
K032434 · Cotronic Manufacturing · Dec 2004
EAR THERMOMETER, MODEL WL-320X
K042631 · Innovatech, Inc. · Dec 2004
MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT18L1
K043110 · Microlife Intellectual Property GmbH · Dec 2004

FDA 510(k) Resources - General Hospital

Additional regulatory intelligence related to this FDA 510(k) submission, including predicate strategy, review pathways and device classification guidance.