Tak Ent., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tak Ent., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Tak Ent., Inc. has 4 FDA 510(k) cleared medical devices. Based in Walnut, US.
Historical record: 4 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tak Ent., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tak Ent., Inc.
4 devices
Cleared
May 22, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
66d
Cleared
Apr 26, 1989
PATIENT EXAMINATION GLOVES (VINYL)
General Hospital
34d
Cleared
Apr 25, 1989
TAK, VINYL PATIENT EXAMINATION GLOVES
General Hospital
39d
Cleared
Apr 13, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
27d