Kit Pak, Inc. - FDA 510(k) Cleared Devices
13
Total
4
Cleared
0
Denied
Kit Pak, Inc. has 4 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.
Historical record: 4 cleared submissions from 1989 to 1995. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Kit Pak, Inc. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Feb 14, 1995
KIT PAK WET SALINE DRESSING
General & Plastic Surgery
236d
Cleared
Jul 20, 1994
KIT PAK DRESSING CHANGE TRAY
General Hospital
113d
Cleared
Jun 01, 1994
KIT PAK INCONTINENT SKIN CARE KIT
Gastroenterology & Urology
386d
Cleared
May 18, 1994
URINARY DRAINAGE BAG
Gastroenterology & Urology
271d
Cleared
Aug 09, 1993
FOLEY CATHETER TRAY
Gastroenterology & Urology
164d
Cleared
Jul 02, 1993
WOUND DRESSING KIT
General & Plastic Surgery
332d
Cleared
Jun 22, 1993
FOLEY INSERTION TRAY
Gastroenterology & Urology
322d
Cleared
Jun 22, 1993
KIT PAK I.V. START KIT
General Hospital
314d
Cleared
Jun 17, 1993
KIT PAK'S FLUSHING KIT
Gastroenterology & Urology
412d
Cleared
Apr 19, 1993
KIT PAK URINARY CARE SUPPLIES
Gastroenterology & Urology
181d
Cleared
Apr 23, 1990
KIT PAK IRRIGATION TRAY
General & Plastic Surgery
102d
Cleared
May 05, 1989
SKIN SCRUB KIT
General & Plastic Surgery
88d
Cleared
Jan 09, 1989
KIT PAK SUCTION CATHETER KIT
Anesthesiology
28d