Medical Device Manufacturer · US , Roswell , GA

H. Bernath & Assoc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

Total

Cleared

Denied

H. Bernath & Assoc. has 1 FDA 510(k) cleared medical devices. Based in Roswell, US.

Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by H. Bernath & Assoc. Filter by specialty or product code using the sidebar.

H. Bernath & Assoc. 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 - H. Bernath & Assoc.

1 devices

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