FDA 510(k)

Image Quality Analyzer (IQA)

Número K: K200422 · 2020-12-24

Data da decisão2020-12-24

Código do produtoNFJ

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Image Quality Analyzer (IQA) is the device name listed in this FDA 510(k) record. The listed applicant is Visionquest Biomedical, Inc.. It received FDA 510(k) clearance on 2020-12-24 under 510(k) number K200422. The device is classified under product code NFJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Image Quality Analyzer (IQA)?

Image Quality Analyzer (IQA) is a medical device that received FDA 510(k) clearance on 2020-12-24. The listed applicant is Visionquest Biomedical, Inc.. The 510(k) number is K200422.

When did Image Quality Analyzer (IQA) receive FDA 510(k) clearance?

Image Quality Analyzer (IQA) received FDA 510(k) clearance on 2020-12-24, under 510(k) number K200422.

Who is the listed applicant for Image Quality Analyzer (IQA)?

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

What is the FDA product code for Image Quality Analyzer (IQA)?

The FDA product code for Image Quality Analyzer (IQA) is NFJ.

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