Cleared Traditional

K023500 - DIGITAL CLINICAL THERMOMETER, MODEL BABY TEMP/WL-3305 AND BABY TEMP (+) /WL-3306

K023500 is an FDA 510(k) clearance for DIGITAL CLINICAL THERMOMETER, manufactured by Innovatech, Inc.. The device is a Class 2 General Hospital device with product code FLL cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K023500 · Innovatech, Inc. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Dec 2002
Decision
56d
Days
Class 2
Risk

K023500 is an FDA 510(k) clearance for the DIGITAL CLINICAL THERMOMETER, MODEL BABY TEMP/WL-3305 AND BABY TEMP (+) /WL-3306. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by Innovatech, Inc. (Pei Tun Dist. Taichung, TW). The FDA issued a Cleared decision on December 13, 2002 after a review of 56 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.

FDA 510(k) Submission Details - K023500

510(k) Number K023500 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 18, 2002
Decision Date December 13, 2002
Days to Decision 56 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 129d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 Peers - FLL Continuous Measurement Thermometer

All 738
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K023500.
JASUN, MODELS DT-01F AND DT-11F
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TRUTEK SELECT MODEL TT-1001
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DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE
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TIMEX ACCUCURVE TALKING 30 SECOND THERMOMTER
K023538 · Medport, Inc. · Nov 2002
TIMEX DIGITAL ORAL THERMOMETERS
K023069 · Medport, Inc. · Oct 2002
K023500 · DIGITAL CLINICAL THERMOMETER, MODEL BABY TEMP/WL-3305 AND BABY TEMP (+) /WL-3306
Download PDF FDA Summary Innovatech, Inc.