Acmi Corporation - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Acmi Corporation Gastroenterology & Urology ✕
10 devices
Cleared
Mar 31, 2006
ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
Gastroenterology & Urology
58d
Cleared
Sep 02, 2005
UROPASS URETERAL ACCESS SHEATH, MODEL 61224
Gastroenterology & Urology
78d
Cleared
Aug 16, 2005
ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL
Gastroenterology & Urology
19d
Cleared
Mar 03, 2005
DUAL LUMEN CATHETER
Gastroenterology & Urology
65d
Cleared
Sep 10, 2004
ACMI INVISIO ICN, MODELS ICN-0564 AND ICN-0565
Gastroenterology & Urology
24d
Cleared
Sep 02, 2003
ACMI M4 TELESCOPES
Gastroenterology & Urology
88d
Cleared
Jul 16, 2003
ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE
Gastroenterology & Urology
111d
Cleared
Jun 03, 2003
SCOPE GUARD PROTECTIVE SHEATH, MODEL TEL-SH
Gastroenterology & Urology
90d
Cleared
May 21, 2003
ACMI VISTA CTR BIPOLAR LOOP ELECTRODE
Gastroenterology & Urology
51d
Cleared
Jan 03, 2003
USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8
Gastroenterology & Urology
88d