Cleared Traditional

K854800 - NORELCO DIGITAL THERMOMETER, MODEL HT 960

K854800 is an FDA 510(k) clearance for NORELCO DIGITAL THERMOMETER, manufactured by Philips Park. The device is a Class 2 General Hospital device with product code FLL cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K854800 · Philips Park · General Hospital
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Jan 1986
Decision
38d
Days
Class 2
Risk

K854800 is an FDA 510(k) clearance for the NORELCO DIGITAL THERMOMETER, MODEL HT 960. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by Philips Park (Essex, US). The FDA issued a Cleared decision on January 9, 1986 after a review of 38 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 Philips Park devices

FDA 510(k) Submission Details - K854800

510(k) Number K854800 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 1985
Decision Date January 09, 1986
Days to Decision 38 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
91d faster than avg
Panel avg: 129d · This submission: 38d
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 566
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K854800.
SURFACE SKIN TEMP PROBE W/THERMOCOUPLE TYPE T
K864195 · Respiratory Support Products, Inc. · Nov 1986
ESOPHAGEAL/RECTAL TEMPERATURE PROBE W/TYPE T
K864044 · Respiratory Support Products, Inc. · Nov 1986
IVAC MODEL 2080 ELECTRONIC THERMOMETER
K860436 · Y · Feb 1986
TMA TEMPERATURE MONITOR
K852825 · Ferguson Medical · Dec 1985
MON-A-THERM SUBCUTANEOUS TEMP. SENSOR
K853392 · Mon-A-Therm, Inc. · Nov 1985
YSI MODEL 790 TELE-THERMOMETER
K853551 · Yellow Springs Instrument Co., Inc. · Sep 1985