FDA 510(k) Applications Submitted by ACMI CORPORATION
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K030684 |
03/05/2003 |
SCOPE GUARD PROTECTIVE SHEATH, MODEL TEL-SH |
ACMI CORPORATION |
| K030935 |
03/25/2003 |
BERKELEY V-10 VACUUM CURETTAGE SYSTEM |
ACMI CORPORATION |
| K012018 |
06/28/2001 |
BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910 |
ACMI CORPORATION |
| K031001 |
03/31/2003 |
ACMI VISTA CTR BIPOLAR LOOP ELECTRODE |
ACMI CORPORATION |
| K031758 |
06/06/2003 |
ACMI M4 TELESCOPES |
ACMI CORPORATION |
| K051593 |
06/16/2005 |
UROPASS URETERAL ACCESS SHEATH, MODEL 61224 |
ACMI CORPORATION |
| K043581 |
12/28/2004 |
DUAL LUMEN CATHETER |
ACMI CORPORATION |
| K030960 |
03/27/2003 |
ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE |
ACMI CORPORATION |
| K022480 |
07/26/2002 |
ACMI DISPOSABLE BIPOLAR CORD, MODEL DBC |
ACMI CORPORATION |
| K060752 |
03/21/2006 |
ACMI DUR-HL LASER SYSTEMS |
ACMI CORPORATION |
| K023358 |
10/07/2002 |
USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8 |
ACMI CORPORATION |
| K060269 |
02/01/2006 |
ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM |
ACMI CORPORATION |
| K061975 |
07/13/2006 |
PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK |
ACMI CORPORATION |
| K052044 |
07/28/2005 |
ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL |
ACMI CORPORATION |
| K042069 |
08/02/2004 |
INVISIO IRL DIGITAL RIGID LAPAROSCOPE SYSTEM |
ACMI CORPORATION |
| K042225 |
08/17/2004 |
ACMI INVISIO ICN, MODELS ICN-0564 AND ICN-0565 |
ACMI CORPORATION |
|
|
