FDA 510(k)

BRS Procedure Face Mask

Número K: K202824 · 2021-03-25

RequerenteBlackbriar Regulatory Services, LLC

Data da decisão2021-03-25

Código do produtoFXX

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

BRS Procedure Face Mask is the device name listed in this FDA 510(k) record. The listed applicant is Blackbriar Regulatory Services, LLC. It received FDA 510(k) clearance on 2021-03-25 under 510(k) number K202824. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the BRS Procedure Face Mask?

BRS Procedure Face Mask is a medical device that received FDA 510(k) clearance on 2021-03-25. The listed applicant is Blackbriar Regulatory Services, LLC. The 510(k) number is K202824.

When did BRS Procedure Face Mask receive FDA 510(k) clearance?

BRS Procedure Face Mask received FDA 510(k) clearance on 2021-03-25, under 510(k) number K202824.

Who is the listed applicant for BRS Procedure Face Mask?

The FDA 510(k) record lists Blackbriar Regulatory Services, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRS Procedure Face Mask?

The FDA product code for BRS Procedure Face Mask is FXX.

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