Cleared Traditional

K110559 - AVITA INFRARED THEROMETER WITH BLUETOOTH
(FDA 510(k) Clearance)

Jan 2012
Decision
312d
Days
Class 2
Risk

K110559 is an FDA 510(k) clearance for the AVITA INFRARED THEROMETER WITH BLUETOOTH. This device is classified as a Continuous Measurement Thermometer (Class II - Special Controls, product code FLL).

Submitted by Avita Corporation (Flagstaff, US). The FDA issued a Cleared decision on January 6, 2012, 312 days after receiving the submission on February 28, 2011.

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 K110559 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 28, 2011
Decision Date January 06, 2012
Days to Decision 312 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement

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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