Continental Medical Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PROD. NO. 01-132 - SUTURE REMOVAL KIT, STAPLE REMOVAL KIT, PROD. NO. 02-031 - LACERATION TRAY
8
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Continental Medical Laboratories, Inc. General Hospital ✕
1 devices