Cleared Traditional

K101912 - THE INFRARED FOREHEAD THERMOMETER, MODEL FS-300&301

K101912 is an FDA 510(k) clearance for THE INFRARED FOREHEAD THERMOMETER, manufactured by Hubdic Co., Ltd.. The device is a Class 2 General Hospital device with product code FLL cleared through the Traditional 510(k) pathway after a 124-day FDA review.

K101912 · Hubdic Co., Ltd. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2010
Decision
124d
Days
Class 2
Risk

K101912 is an FDA 510(k) clearance for the THE INFRARED FOREHEAD THERMOMETER, MODEL FS-300&301. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by Hubdic Co., Ltd. (Pittsburgh, US). The FDA issued a Cleared decision on November 10, 2010 after a review of 124 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K101912

510(k) Number K101912 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 09, 2010
Decision Date November 10, 2010
Days to Decision 124 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
5d faster than avg
Panel avg: 129d · This submission: 124d
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 794
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K101912.
DIGITAL THERMOMETER
K102718 · International Regulatory Consultants, LLC (Irc) · Dec 2010
RII INFRARED EAR THERMOMETER,
K102187 · Radiant Innovation, Inc. · Dec 2010
SKIN SENSOR PROBE, GENERAL PURPOSE PROBE, TYMPANIC PROBE
K101244 · Truer Medical, Inc. · Nov 2010
INFRARED EAR THERMOMETER MODEL DR. SCHVEN ICT-1000
K100660 · Innochips Technology Co., Ltd. · Oct 2010
ABREU, MODEL 700
K100843 · Brain Tunnelgenix Technologies Corp · Aug 2010
BRAUN THERMOSCAN PRO 4000 SERIES AND BRAUN THERMOSCAN IRT 4000 SERIES MODEL 6021791-PRO 4000 SERIES, 6022790-IRT 4000 SE
K101747 · Kaz USA, Inc (A Subsidiaryof Kaz Inc) · Aug 2010
K101912 · THE INFRARED FOREHEAD THERMOMETER, MODEL FS-300&301
Download PDF FDA Summary Hubdic Co., Ltd.