| K-number | K833021 |
| Device name | PERI-GUARD PERICARDIAL PATCH-HERNIA |
| Applicant | Genetic |
| Product code | DXZ |
| Device class | Class II |
| Decision date | Dec 26, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 870.3470 |
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