Pacesetter, Inc. · Class III · Cleared Feb 1, 1996
| K-number | K954714 |
| Device name | AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION) |
| Applicant | Pacesetter, Inc. |
| Product code | DTB |
| Device class | Class III |
| Decision date | Feb 1, 1996 |
| Decision | Substantially Equivalent - Subject to Tracking Reg. |
| 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