FDA 510(k)

nva, nvp, and nvt

Número K: K162426 · 2016-09-29

RequerenteNvision Biomedical Technologies, LLC

Data da decisão2016-09-29

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

nva, nvp, and nvt is the device name listed in this FDA 510(k) record. The listed applicant is Nvision Biomedical Technologies, LLC. It received FDA 510(k) clearance on 2016-09-29 under 510(k) number K162426. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the nva, nvp, and nvt?

nva, nvp, and nvt is a medical device that received FDA 510(k) clearance on 2016-09-29. The listed applicant is Nvision Biomedical Technologies, LLC. The 510(k) number is K162426.

When did nva, nvp, and nvt receive FDA 510(k) clearance?

nva, nvp, and nvt received FDA 510(k) clearance on 2016-09-29, under 510(k) number K162426.

Who is the listed applicant for nva, nvp, and nvt?

The FDA 510(k) record lists Nvision Biomedical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for nva, nvp, and nvt?

The FDA product code for nva, nvp, and nvt is MAX.

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Fonte oficial

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