The following data is part of a premarket notification filed by Siemens Elema Ab with the FDA for Siemens-elema Pulse Generator 678.
| Device ID | K802864 |
| 510k Number | K802864 |
| Device Name: | SIEMENS-ELEMA PULSE GENERATOR 678 |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | SIEMENS ELEMA AB 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 | 1980-11-12 |
| Decision Date | 1981-02-05 |