The following data is part of a premarket notification filed by Pacesetter Systems with the FDA for Afp Model 262t Pulse Generator.
| Device ID | K884733 |
| 510k Number | K884733 |
| Device Name: | AFP MODEL 262T PULSE GENERATOR |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | PACESETTER SYSTEMS 12884 BRADLEY AVE. Sylmar, CA 91342 |
| Contact | Rita Brown |
| Correspondent | Rita Brown PACESETTER SYSTEMS 12884 BRADLEY AVE. Sylmar, CA 91342 |
| Product Code | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-11-10 |
| Decision Date | 1989-02-10 |