FDA 510(k)

D Camera Controller

Número K: K211332 · 2021-10-01

RequerenteRichard Wolf Medical Instruments Corporation

Data da decisão2021-10-01

Código do produtoFET

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

D Camera Controller is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corporation. It received FDA 510(k) clearance on 2021-10-01 under 510(k) number K211332. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the D Camera Controller?

D Camera Controller is a medical device that received FDA 510(k) clearance on 2021-10-01. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K211332.

When did D Camera Controller receive FDA 510(k) clearance?

D Camera Controller received FDA 510(k) clearance on 2021-10-01, under 510(k) number K211332.

Who is the listed applicant for D Camera Controller?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for D Camera Controller?

The FDA product code for D Camera Controller is FET.

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Fonte oficial

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