Cobe Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATOR, COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTIC, COBE CENTRY 2 BICART OPTION KIT
77
Total
77
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cobe Laboratories, Inc. General & Plastic Surgery ✕
2 devices