Intermedics, Inc. · Class III · Cleared Sep 6, 1988
| K-number | K883602 |
| Device name | BIOPORE VS.1 ENDOCARDIAL INTER IMPLANT PACING LEAD |
| Applicant | Intermedics, Inc. |
| Product code | DTB |
| Device class | Class III |
| Decision date | Sep 6, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 870.3680 |
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