Pearce Clinical Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pearce Clinical Laboratories, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Pearce Clinical Laboratories, Inc. has 3 FDA 510(k) cleared medical devices. Based in Conroe, US.
Historical record: 3 cleared submissions from 1987 to 1988.
Browse the FDA 510(k) cleared devices submitted by Pearce Clinical Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pearce Clinical Laboratories, Inc.
3 devices