Cutter Laboratories, Inc. · Class I · Cleared Dec 10, 1979
| K-number | K792207 |
| Device name | PERIDIAL PERITONEAL DIALYSIS TRAY |
| Applicant | Cutter Laboratories, Inc. |
| Product code | FKG |
| Device class | Class I |
| Decision date | Dec 10, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 876.5820 |
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