Cleared Traditional

K211744 - Non-Contact Infrared Thermometer

K211744 is the FDA 510(k) clearance for Non-Contact Infrared Thermometer by Health & Life Co., Ltd.. It is a Class 2 General Hospital device (product code FLL) cleared through the Traditional 510(k) pathway after a 170-day FDA review.

K211744 · Health & Life Co., Ltd. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2021
Decision
170d
Days
Class 2
Risk

K211744 is an FDA 510(k) clearance for the Non-Contact Infrared Thermometer, model HL710H. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by Health & Life Co., Ltd. (New Taipei, TW). The FDA issued a Cleared decision on November 24, 2021 after a review of 170 days - an extended review 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: 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.

View all Health & Life Co., Ltd. devices

Submission Details

510(k) Number K211744 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 07, 2021
Decision Date November 24, 2021
Days to Decision 170 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
41d slower than avg
Panel avg: 129d · This submission: 170d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 317
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K211744.
Circa S-Cath M Esophageal Temperature Probe and Temperature Monitoring System
K200943 · Circa Scientific, LLC · Dec 2021
Infrared thermometer, models KFT-22M, KFT-22, KFT-23, KFT-24, KFT-25, KFT-26, KFT-27, KFT-28
K201600 · Kangfu Medical Equipment Factory · Dec 2021
Infrared forehead thermometer LD-FT-100B
K211629 · Honsun (Nantong) Co., Ltd. · Dec 2021
Phoenix Digital Thermometer
K201032 · Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd. · Oct 2021
Infrared Thermometer (Model K9)
K203497 · Kangzhan Communication Electronics Co., Ltd. · Oct 2021
ThermArt (Model IR-EFT)
K202481 · Comper Chuangxiang (Beijing) Technology Co., Ltd. · Sep 2021