Scanlan Intl., Inc. - FDA 510(k) Cleared Devices
Recent clearances: SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM, SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER, SCANLAN/TAHERI VALVULOTOME
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Scanlan Intl., Inc. General Hospital ✕
1 devices