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FDA 510(k)

LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)

Número K: K172011 · 2018-06-14

RequerenteHmicro, Inc.
Data da decisão2018-06-14
Código do produtoDRG
Comité consultivoCV
DecisãoSubstantially Equivalent

Resumo do dispositivo

LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) is the device name listed in this FDA 510(k) record. The listed applicant is Hmicro, Inc.. It received FDA 510(k) clearance on 2018-06-14 under 510(k) number K172011. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)?

LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) is a medical device that received FDA 510(k) clearance on 2018-06-14. The listed applicant is Hmicro, Inc.. The 510(k) number is K172011.

When did LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) receive FDA 510(k) clearance?

LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) received FDA 510(k) clearance on 2018-06-14, under 510(k) number K172011.

Who is the listed applicant for LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)?

The FDA 510(k) record lists Hmicro, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System)?

The FDA product code for LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) is DRG.

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Fonte oficial

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