Dukal Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dukal Corp. - FDA 510(k) Cleared Devices
11
Total
10
Cleared
0
Denied
Dukal Corp. has 10 FDA 510(k) cleared medical devices. Based in Clinton, US.
Historical record: 10 cleared submissions from 1993 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dukal Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dukal Corp.
11 devices
Cleared
Mar 06, 2009
DUKAL SURGICAL DRAPE
General Hospital
114d
Cleared
Mar 26, 2007
DUKAL SURGICAL FACE MASK TIE, EAR LOOP, WITH SHIELD YELLOW & WHITE
General Hospital
42d
Cleared
Sep 15, 2006
DUKAL SURGICAL FACE MASK TIE-ON, MODEL 1530
General Hospital
74d
Cleared
May 15, 2002
DUKAL DISPOSABLE VAGINAL SPECULUM, SMALL, MEDIUM, AND LARGE
Obstetrics & Gynecology
70d
Cleared
Dec 02, 1999
ETHYL CHLORIDE DISPENSER
Physical Medicine
344d
Cleared
May 08, 1997
DUKAL NON ADHERENT DRESSING
General & Plastic Surgery
91d
Cleared
May 08, 1997
DUKAL ABD COMBINE PAD
General & Plastic Surgery
91d
Cleared
Jan 18, 1996
DUKAL TRANSPARENT WOUND DRESSING
General & Plastic Surgery
49d
Cleared
Mar 09, 1994
DUKAL NON-WOVEN GAUZE
General & Plastic Surgery
37d
Cleared
Feb 02, 1994
GAUZE SPONGE
General & Plastic Surgery
42d
Cleared
Jul 14, 1993
DUKAL SKIN CLOSURE STRIP
General & Plastic Surgery
138d