The Buckeye Cellulose Corp.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K822925 | BOUNDARY SINGLE-USE GOWNS | FYA | 1983-01-12 | View |
| 510(k) | K823173 | ARRIRM SCRUB BRUSH/SPONGE | GEC | 1982-11-22 | View |
| 510(k) | K821564 | BOUNDARY PROCESS CHANGE | FYA | 1982-07-02 | View |
| 510(k) | K820758 | BOUNDARY SINGLE-USE CRANIOTOMY SHEET | KKX | 1982-04-29 | View |
| 510(k) | K820116 | BOUNDARY | FYA | 1982-02-23 | View |
| 510(k) | K813450 | BOUNDARY SINGLE-USE DRAPES | KKX | 1982-01-22 | View |
| 510(k) | K813390 | BONDARY SINGLE-USE OR GOWN | FYA | 1982-01-05 | View |
| 510(k) | K813277 | BOUNDARY DRAPE TAPE | KKX | 1981-12-18 | View |
| 510(k) | K813263 | PATIENT UNDERPAD | KME | 1981-11-27 | View |
| 510(k) | K812962 | BOUNDARY SURGICAL DRAPE | KKX | 1981-11-20 | View |
| 510(k) | K812738 | BOUNDARY PROCESS CHANGE | KKX | 1981-11-16 | View |
| 510(k) | K811819 | BOUNDARY STERILIZATION WRAP | FRG | 1981-08-04 | View |
| 510(k) | K811958 | BOUNDARY REINFORCED OR GOWN | FYA | 1981-07-27 | View |
| 510(k) | K810888 | BOUNDARY TUBING HOLDERS | FZX | 1981-04-23 | View |
| 510(k) | K803158 | IRRADIATED BOUNDARY DEVICES | FYA | 1981-01-15 | View |
| 510(k) | K801768 | CONTAIN X-RAY DETECTABLE LAP SPONGE | GDY | 1980-08-20 | View |
| 510(k) | K801024 | ODOR MASKING AGENT IN BOUNDARY OBSTETRI. | HHL | 1980-07-28 | View |
| 510(k) | K801025 | ODOR MASKING AGENT FOR CONTENTS OF ALL | FYA | 1980-05-30 | View |
No matching devices.
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