| K-number | K883984 |
| Device name | HEMORX COLD PACK |
| Applicant | Bio-Dyne, Inc. |
| Product code | LKX |
| Device class | Class U |
| Decision date | Dec 22, 1988 |
| Decision | Substantially Equivalent |
| Regulation | — |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov