Medical Device Manufacturer · US , Crofton , MD

Perfusion Partners & Assoc., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Total

Cleared

Denied

Perfusion Partners & Assoc., Inc. has 2 FDA 510(k) cleared medical devices. Based in Crofton, US.

Historical record: 2 cleared submissions from 2003 to 2007. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Perfusion Partners & Assoc., Inc. Filter by specialty or product code using the sidebar.

Perfusion Partners & Assoc., Inc. 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 - Perfusion Partners & Assoc., Inc.

2 devices

1-2 of 2