Pos-T-Vac, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pos-T-Vac, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Pos-T-Vac, Inc. has 12 FDA 510(k) cleared gastroenterology & urology devices. Based in Dodge City, US.
Historical record: 12 cleared submissions from 1994 to 2002.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pos-T-Vac, Inc.
12 devices
Cleared
Apr 04, 2002
VT-1
Gastroenterology & Urology
77d
Cleared
Apr 04, 2002
SUPPORT SLEEVE
Gastroenterology & Urology
69d
Cleared
Nov 09, 2001
BOSS 2000-3 VACUUM ERECTION DEVICE
Gastroenterology & Urology
88d
Cleared
Nov 09, 2001
BOSS-2000-2 VACUUM ERECTION DEVICE
Gastroenterology & Urology
88d
Cleared
Nov 02, 1998
POS-T-VAC (AVP-1000)
Gastroenterology & Urology
47d
Cleared
Nov 02, 1998
POS-T-VAC (IVP-600)
Gastroenterology & Urology
47d
Cleared
Aug 28, 1998
POS-T-VAC (REJOYN VACUUM ERECTION DEVICE)
Gastroenterology & Urology
163d
Cleared
Aug 28, 1998
REJOYN CONSTRICTION RING KIT, POS-T-VAC B-100 RING KIT, POS-T-VAC B-25 RING...
Gastroenterology & Urology
149d
Cleared
Jun 10, 1996
POS-T-VAC ID-300
General Hospital
67d
Cleared
Mar 08, 1996
POS-T-VAC B-10 BAND KIT
Gastroenterology & Urology
8d
Cleared
Mar 01, 1996
POS-T-VAC AVP-1000 & MVP-700
Gastroenterology & Urology
37d
Cleared
Jul 25, 1994
POS-T-VAC-AVP-1000
Gastroenterology & Urology
139d