Primeline Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PRIMAGARD SURGICAL EQUIPMENT DRAPES, PRIMAGARD SURGICAL GOWNS, PRIMAGARD SURGICAL GOWNS
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Primeline Medical Products, Inc. General & Plastic Surgery ✕
1 devices