Alltek, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alltek, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Alltek, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 5 cleared submissions from 1984 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Alltek, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alltek, Inc.
5 devices
Cleared
Dec 05, 1985
I.V. WATCH
General Hospital
51d
Cleared
May 30, 1985
I.V. WATCH
General Hospital
22d
Cleared
May 30, 1985
PEDIATRIC IV WATCH
General Hospital
22d
Cleared
Jun 19, 1984
MANUAL IRRIGATING/ASPIRATING UNIT
Ophthalmic
134d
Cleared
May 11, 1984
FILTRARE TM ALLVENT TM
General Hospital
149d