Cleared Traditional

K180355 - Advocate Non-Contact Infrared Thermometer (FDA 510(k) Clearance)

Jan 2019
Decision
336d
Days
Class 2
Risk

K180355 is an FDA 510(k) clearance for the Advocate Non-Contact Infrared Thermometer. This device is classified as a Continuous Measurement Thermometer (Class II - Special Controls, product code FLL).

Submitted by Broadmaster Biotech, Corp. (Taoyuan City, TW). The FDA issued a Cleared decision on January 10, 2019, 336 days after receiving the submission on February 8, 2018.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.2910. 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..

Submission Details

510(k) Number K180355 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 08, 2018
Decision Date January 10, 2019
Days to Decision 336 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FLL - Continuous Measurement Thermometer
Device Class Class II - 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.

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