The following data is part of a premarket notification filed by Pacesetter Systems with the FDA for Programalith #'s 221, 222, 221a & 222a.
| Device ID | K801978 |
| 510k Number | K801978 |
| Device Name: | PROGRAMALITH #'S 221, 222, 221A & 222A |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | PACESETTER SYSTEMS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-08-19 |
| Decision Date | 1980-09-26 |