Medical Device Manufacturer · US , Walker , MI

Vitaire Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1976

Total

Cleared

Denied

Vitaire Corp. has 1 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 1 cleared submissions from 1976 to 1976. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Vitaire Corp. Filter by specialty or product code using the sidebar.

Vitaire Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vitaire Corp.

1 devices

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