Medi-Flex Hospital Products, Inc. - FDA 510(k) Cleared Devices
13
Total
9
Cleared
0
Denied
Medi-Flex Hospital Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Overland Park, US.
Historical record: 9 cleared submissions from 1991 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medi-Flex Hospital Products, Inc. Filter by specialty or product code using the sidebar.
13 devices
Cleared
May 09, 1997
K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH
General & Plastic Surgery
93d
Cleared
Sep 06, 1996
DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641
General & Plastic Surgery
53d
Cleared
Oct 04, 1995
PORT-A-CATH ACCESS KIT
General Hospital
147d
Cleared
Aug 09, 1995
TRACHEOSTOMY CARE KIT
Anesthesiology
78d
Cleared
Jul 31, 1995
PICC LINE KIT
General Hospital
77d
Cleared
Jun 08, 1995
ADHEROL SEPP APPLICATOR
General & Plastic Surgery
41d
Cleared
Mar 11, 1994
SEPP ADHESIVE REMOVER
General & Plastic Surgery
157d
Cleared
Jan 25, 1994
COMPOUND BENZOIN TINCTURE USP FREPP
General & Plastic Surgery
726d
Cleared
Jan 25, 1994
COMPOUND BENZOIN TINCTURE USP SEPP
General & Plastic Surgery
586d
Cleared
Jul 02, 1993
CEPTI-SEAL I.V. PREP KIT
General & Plastic Surgery
169d
Cleared
Jan 08, 1993
CEPTI-SEAL DRESSING CHANGE KIT FOR VENOUS CATHETER
General & Plastic Surgery
296d
Cleared
Apr 15, 1992
CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT
General Hospital
76d
Cleared
Dec 24, 1991
CEPTI-SEAL DRESSING CHANGE KIT FOR CENT VEN CATH
General Hospital
89d