The Owenby Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Owenby Co. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
The Owenby Co. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1976 to 1980. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by The Owenby Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Owenby Co.
14 devices
Cleared
Aug 07, 1980
RESTRAINT, PROTECTIVE
Physical Medicine
23d
Cleared
Jul 28, 1980
STOCKINETTE, STERILE TWO PLY W/PULL TABS
General Hospital
27d
Cleared
Jul 28, 1980
ARM SLING
Physical Medicine
13d
Cleared
Jul 28, 1980
COVER, LIMB
Physical Medicine
13d
Cleared
Jul 21, 1980
ARM SLING
Physical Medicine
20d
Cleared
Feb 27, 1979
STOCKINETTE, TUBULAR UNBLEACHED
General Hospital
28d
Cleared
Jun 06, 1978
NON-STERILE FOLDED GAUZE
General & Plastic Surgery
33d
Cleared
Apr 10, 1978
BURN DRESSING PAD
General & Plastic Surgery
27d
Cleared
Jul 11, 1977
BURN DRESSING KIT
General & Plastic Surgery
56d
Cleared
Dec 30, 1976
P.S.M. BOUFFANT CAP
General & Plastic Surgery
44d
Cleared
Dec 30, 1976
P.S.M. BOTIQUE CAP
General & Plastic Surgery
44d
Cleared
Dec 30, 1976
P.S.M. SURGICAL HOOD
General Hospital
44d
Cleared
Dec 30, 1976
P.S.M. JUSTA KAP
General & Plastic Surgery
44d
Cleared
Dec 02, 1976
P.S.M. JUSTA COVER
General Hospital
16d