Acmi Corporation - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Acmi Corporation General & Plastic Surgery ✕
4 devices
Cleared
Aug 10, 2006
PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK
General & Plastic Surgery
28d
Cleared
May 25, 2006
ACMI DUR-HL LASER SYSTEMS
General & Plastic Surgery
65d
Cleared
Nov 01, 2004
INVISIO IRL DIGITAL RIGID LAPAROSCOPE SYSTEM
General & Plastic Surgery
91d
Cleared
Jul 16, 2002
BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910
General & Plastic Surgery
383d