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FDA 510(k)

Shapiro MD model laser 272

Número K: K193667 · 2020-03-25

RequerenteConversion Labs, Pr, LLC
Data da decisão2020-03-25
Código do produtoOAP
Comité consultivoPM
DecisãoSubstantially Equivalent

Resumo do dispositivo

Shapiro MD model laser 272 is the device name listed in this FDA 510(k) record. The listed applicant is Conversion Labs, Pr, LLC. It received FDA 510(k) clearance on 2020-03-25 under 510(k) number K193667. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Shapiro MD model laser 272?

Shapiro MD model laser 272 is a medical device that received FDA 510(k) clearance on 2020-03-25. The listed applicant is Conversion Labs, Pr, LLC. The 510(k) number is K193667.

When did Shapiro MD model laser 272 receive FDA 510(k) clearance?

Shapiro MD model laser 272 received FDA 510(k) clearance on 2020-03-25, under 510(k) number K193667.

Who is the listed applicant for Shapiro MD model laser 272?

The FDA 510(k) record lists Conversion Labs, Pr, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Shapiro MD model laser 272?

The FDA product code for Shapiro MD model laser 272 is OAP.

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