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FDA 510(k)

Phoenix Digital Thermometer

K-Number: K201032 · 2021-10-29

ApplicantPhoenix Innovative Healthcare Manufacturers Pvt. , Ltd.
Decision Date2021-10-29
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Phoenix Digital Thermometer is a medical device manufactured by Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. It received FDA 510(k) clearance on 2021-10-29 under approval number K201032. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Phoenix Digital Thermometer?

Phoenix Digital Thermometer is a medical device that received FDA 510(k) clearance on 2021-10-29. It is manufactured by Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.. The 510(k) number is K201032.

When was Phoenix Digital Thermometer approved by the FDA?

Phoenix Digital Thermometer received FDA 510(k) clearance on 2021-10-29, under approval number K201032.

What company makes Phoenix Digital Thermometer?

Phoenix Digital Thermometer is manufactured by Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd..

What is the FDA product code for Phoenix Digital Thermometer?

The FDA product code for Phoenix Digital Thermometer is FLL.

Other Devices by Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.

K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)

Related Devices (Code: FLL)

K160306Cloud Smart ThermometerGuangzhou Bosma Technology Co, Ltd. K161728Microlife Digital Infrared Forehead Thermometer, Model FR1MN1-1Microfile Intellectual Property GmbH K161735Non-contact Forehead ThermometerShenzhen Dongdixin Technology Co., Ltd. K160816Infrared Thermometer (Model: LX-26E, LX-260TE, PRO LX-261E, LX-360, LX-361T, BW-CX10)Nexmed Technology Co., Ltd. K161211Digital ThermometerBiocare Asia Corporation , Ltd. K160802Infrared Forehead Thermometer, FT-100AHangzhou Universal Electronic Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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