FDA 510(k)

Single-Use Flexible Rhinolaryngoscope

Número K: K221581 · 2022-11-18

RequerenteHunan Vathin Medical Instrument Co., Ltd.

Data da decisão2022-11-18

Código do produtoEOB

Comité consultivoEN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Single-Use Flexible Rhinolaryngoscope is the device name listed in this FDA 510(k) record. The listed applicant is Hunan Vathin Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2022-11-18 under 510(k) number K221581. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Single-Use Flexible Rhinolaryngoscope?

Single-Use Flexible Rhinolaryngoscope is a medical device that received FDA 510(k) clearance on 2022-11-18. The listed applicant is Hunan Vathin Medical Instrument Co., Ltd.. The 510(k) number is K221581.

When did Single-Use Flexible Rhinolaryngoscope receive FDA 510(k) clearance?

Single-Use Flexible Rhinolaryngoscope received FDA 510(k) clearance on 2022-11-18, under 510(k) number K221581.

Who is the listed applicant for Single-Use Flexible Rhinolaryngoscope?

The FDA 510(k) record lists Hunan Vathin Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Single-Use Flexible Rhinolaryngoscope?

The FDA product code for Single-Use Flexible Rhinolaryngoscope is EOB.

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Outros registros que listam Hunan Vathin Medical Instrument Co., Ltd. como candidato(a)

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Fonte oficial

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