Beech Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beech Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Beech Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 5 cleared submissions from 1982 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Beech Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beech Medical, Inc.
5 devices
Cleared
Dec 29, 1993
BEECH PROLOK
General Hospital
149d
Cleared
Apr 28, 1983
MINI-VOL EXTENSION SET
General Hospital
24d
Cleared
Apr 28, 1983
MINI-VOL I.V. SET
General Hospital
24d
Cleared
Apr 28, 1983
INFUSION PUMP
General Hospital
24d
Cleared
Dec 30, 1982
BENZING RETROGRADE ADMIN. SET
General Hospital
48d