Kit Pak, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Kit Pak, Inc.
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