FDA 510(k) Applications Submitted by JOHN NICHOLSON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040138 |
01/22/2004 |
VICEROY INFLATION DEVICE |
MERIT MEDICAL SYSTEMS, INC. |
| K983525 |
10/08/1998 |
GORE REVOX THYROPLASTY IMPLANT |
W.L. GORE & ASSOCIATES,INC |
| K984534 |
12/21/1998 |
PRECLUDE ACUSEAL DURA SUBSTITUTE |
W.L. GORE & ASSOCIATES,INC |
| K960656 |
02/15/1996 |
GORE BURR HOLE COVER |
W.L. GORE & ASSOCIATES,INC |
| K981051 |
03/18/1998 |
SOFT TISSUE PATCH PLUS, DUALMESH PLUS, MYCROMESH PLUS, DUALMESH PLUS WITH HOLES |
W.L. GORE & ASSOCIATES,INC |
| K961210 |
03/28/1996 |
SAM FACIAL IMPLANT |
W.L. GORE & ASSOCIATES,INC |
| K961802 |
05/09/1996 |
PRECLUDE SYNBLOC MEMBRANE |
W.L. GORE & ASSOCIATES,INC |
| K962241 |
06/11/1996 |
GORE SPHEREX IMPLANT |
W.L. GORE & ASSOCIATES,INC |
| K031922 |
06/23/2003 |
CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W |
MERIT MEDICAL SYSTEMS, INC. |
| K963619 |
09/10/1996 |
GORE-TEX SOFT TISSUE PATCH,MYCROMESHA BIOMATERIAL,DUALMESH BIOMATERIAL,DUALMESH BIOMATERIAL WITH HOLES |
W.L. GORE & ASSOCIATES,INC |
| K973594 |
09/22/1997 |
GORE RESOLUT XT REGENERATIVE MATERIAL |
W.L. GORE & ASSOCIATES,INC |
| K964761 |
11/27/1996 |
S.A.M. FACIAL IMPLANT W/INTRODUCER |
W.L. GORE & ASSOCIATES,INC |
| K955494 |
12/01/1995 |
GORE-TEX DUALMESH BIOMATERIAL WITH HOLES |
W.L. GORE & ASSOCIATES,INC |
| K073559 |
12/19/2007 |
18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA II |
EDWARDS LIFESCIENCES RESEARCH MEDICAL |
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