Cleared Special

K102187 - RII INFRARED EAR THERMOMETER,

K102187 is an FDA 510(k) clearance for RII INFRARED EAR THERMOMETER, manufactured by Radiant Innovation, Inc.. The device is a Class 2 General Hospital device with product code FLL cleared through the Special 510(k) pathway after a 129-day FDA review.

K102187 · Radiant Innovation, Inc. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Dec 2010
Decision
129d
Days
Class 2
Risk

K102187 is an FDA 510(k) clearance for the RII INFRARED EAR THERMOMETER,. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by Radiant Innovation, Inc. (Hsinchu, TW). The FDA issued a Cleared decision on December 10, 2010 after a review of 129 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.2910 - the FDA general hospital device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

FDA 510(k) Submission Details - K102187

510(k) Number K102187 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 03, 2010
Decision Date December 10, 2010
Days to Decision 129 days
Submission Type Special
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
At panel average
Panel avg: 129d · This submission: 129d
Pathway characteristics
Modification to existing cleared device.

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 794
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K102187.
YU LONG SHENG DISPOSABLE THERMOMETER SHEATHS, MODELS YLS-01 AND YLS-02
K102508 · Yu Long Sheng Technology Co., Ltd. · Jan 2011
INFRARED EAR THERMOMETER
K103097 · Radiant Innovation, Inc. · Dec 2010
DIGITAL THERMOMETER
K102718 · International Regulatory Consultants, LLC (Irc) · Dec 2010
SKIN SENSOR PROBE, GENERAL PURPOSE PROBE, TYMPANIC PROBE
K101244 · Truer Medical, Inc. · Nov 2010
THE INFRARED FOREHEAD THERMOMETER, MODEL FS-300&301
K101912 · Hubdic Co., Ltd. · Nov 2010
INFRARED EAR THERMOMETER MODEL DR. SCHVEN ICT-1000
K100660 · Innochips Technology Co., Ltd. · Oct 2010
K102187 · RII INFRARED EAR THERMOMETER,
Download PDF FDA Summary Radiant Innovation, I…