FDA 510(k)

SPiN Vision Video Bronchoscope System

Número K: K202346 · 2021-02-19

RequerenteVeran Medical Technologies, Inc.

Data da decisão2021-02-19

Código do produtoEOQ

Comité consultivoEN

DecisãoSubstantially Equivalent

Resumo do dispositivo

SPiN Vision Video Bronchoscope System is the device name listed in this FDA 510(k) record. The listed applicant is Veran Medical Technologies, Inc.. It received FDA 510(k) clearance on 2021-02-19 under 510(k) number K202346. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SPiN Vision Video Bronchoscope System?

SPiN Vision Video Bronchoscope System is a medical device that received FDA 510(k) clearance on 2021-02-19. The listed applicant is Veran Medical Technologies, Inc.. The 510(k) number is K202346.

When did SPiN Vision Video Bronchoscope System receive FDA 510(k) clearance?

SPiN Vision Video Bronchoscope System received FDA 510(k) clearance on 2021-02-19, under 510(k) number K202346.

Who is the listed applicant for SPiN Vision Video Bronchoscope System?

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

What is the FDA product code for SPiN Vision Video Bronchoscope System?

The FDA product code for SPiN Vision Video Bronchoscope System is EOQ.

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Dispositivos Relacionados (Código: EOQ)

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Fonte oficial

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