FDA 510(k) Applications Submitted by TERRENCE E SULLIVAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K023358 |
10/07/2002 |
USA SERIES DUR 8 ELITE, USA SERIES DUR 8, MODELS DUR 8E, DUR 8 |
ACMI CORPORATION |
| K080093 |
01/14/2008 |
PKS PLASMA MORCELLATOR, MODELS 962000PK, 3620PK |
GYRUS ACMI, INC. |
| K060269 |
02/01/2006 |
ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM |
ACMI CORPORATION |
| K081954 |
07/09/2008 |
GYRUS ACMI GENERAL SURGERY WORKSTATION, MODEL G400, AND DUAL FOOTSWITCH CONNECTOR CABLE |
GYRUS ACMI, INC. |
| K061975 |
07/13/2006 |
PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK |
ACMI CORPORATION |
| K082054 |
07/21/2008 |
GYRUS ACMI PLASMAKINETIC (PK) SUPERPULSE SYSTEM, MODEL 744000 AND DUAL FOOTSWITCH CONNECTOR CABLE, MODEL 710003 |
GYRUS ACMI, INC. |
| 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 |
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