The Kendall Company, L.P. - FDA 510(k) Cleared Devices
Recent clearances: KERLIX MD ANTIMICROBIAL GAUZE DRESSING, KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - The Kendall Company, L.P. General & Plastic Surgery ✕
1 devices