Medical Device Manufacturer · US , Greenwood , SC

Paul Hartmann Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1984

Total

Cleared

Denied

Paul Hartmann Corp. has 5 FDA 510(k) cleared medical devices. Based in Greenwood, US.

Historical record: 5 cleared submissions from 1984 to 1984. Primary specialty: Gastroenterology & Urology.

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

Paul Hartmann 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 - Paul Hartmann Corp.

5 devices

1-5 of 5