Company ยท US
The Buckeye Cellulose Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1983. Name variants (Inc, Corp, punctuation) are merged.
18510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 12, 1983 | K822925 | BOUNDARY SINGLE-USE GOWNS The Buckeye Cellulose Corp. | FYA |
| Nov 22, 1982 | K823173 | ARRIRM SCRUB BRUSH/SPONGE The Buckeye Cellulose Corp. | GEC |
| Jul 2, 1982 | K821564 | BOUNDARY PROCESS CHANGE The Buckeye Cellulose Corp. | FYA |
| Apr 29, 1982 | K820758 | BOUNDARY SINGLE-USE CRANIOTOMY SHEET The Buckeye Cellulose Corp. | KKX |
| Feb 23, 1982 | K820116 | BOUNDARY The Buckeye Cellulose Corp. | FYA |
| Jan 22, 1982 | K813450 | BOUNDARY SINGLE-USE DRAPES The Buckeye Cellulose Corp. | KKX |
| Jan 5, 1982 | K813390 | BONDARY SINGLE-USE OR GOWN The Buckeye Cellulose Corp. | FYA |
| Dec 18, 1981 | K813277 | BOUNDARY DRAPE TAPE The Buckeye Cellulose Corp. | KKX |
| Nov 27, 1981 | K813263 | PATIENT UNDERPAD The Buckeye Cellulose Corp. | KME |
| Nov 20, 1981 | K812962 | BOUNDARY SURGICAL DRAPE The Buckeye Cellulose Corp. | KKX |
| Nov 16, 1981 | K812738 | BOUNDARY PROCESS CHANGE The Buckeye Cellulose Corp. | KKX |
| Aug 4, 1981 | K811819 | BOUNDARY STERILIZATION WRAP The Buckeye Cellulose Corp. | FRG |
| Jul 27, 1981 | K811958 | BOUNDARY REINFORCED OR GOWN The Buckeye Cellulose Corp. | FYA |
| Apr 23, 1981 | K810888 | BOUNDARY TUBING HOLDERS The Buckeye Cellulose Corp. | FZX |
| Jan 15, 1981 | K803158 | IRRADIATED BOUNDARY DEVICES The Buckeye Cellulose Corp. | FYA |
| Aug 20, 1980 | K801768 | CONTAIN X-RAY DETECTABLE LAP SPONGE The Buckeye Cellulose Corp. | GDY |
| Jul 28, 1980 | K801024 | ODOR MASKING AGENT IN BOUNDARY OBSTETRI. The Buckeye Cellulose Corp. | HHL |
| May 30, 1980 | K801025 | ODOR MASKING AGENT FOR CONTENTS OF ALL The Buckeye Cellulose Corp. | FYA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||