The Buckeye Cellulose Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Buckeye Cellulose Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
The Buckeye Cellulose Corp. has 18 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1980 to 1983.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Buckeye Cellulose Corp.
18 devices
Cleared
Jan 12, 1983
BOUNDARY SINGLE-USE GOWNS
General Hospital
103d
Cleared
Nov 22, 1982
ARRIRM SCRUB BRUSH/SPONGE
General & Plastic Surgery
27d
Cleared
Jul 02, 1982
BOUNDARY PROCESS CHANGE
General Hospital
38d
Cleared
Apr 29, 1982
BOUNDARY SINGLE-USE CRANIOTOMY SHEET
General Hospital
38d
Cleared
Feb 23, 1982
BOUNDARY
General Hospital
36d
Cleared
Jan 22, 1982
BOUNDARY SINGLE-USE DRAPES
General Hospital
43d
Cleared
Jan 05, 1982
BONDARY SINGLE-USE OR GOWN
General Hospital
33d
Cleared
Dec 18, 1981
BOUNDARY DRAPE TAPE
General Hospital
25d
Cleared
Nov 27, 1981
PATIENT UNDERPAD
General Hospital
7d
Cleared
Nov 20, 1981
BOUNDARY SURGICAL DRAPE
General Hospital
29d
Cleared
Nov 16, 1981
BOUNDARY PROCESS CHANGE
General Hospital
48d
Cleared
Aug 04, 1981
BOUNDARY STERILIZATION WRAP
General Hospital
36d