The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Siemens-elema Pulse Generator 668 B.
| Device ID | K812610 |
| 510k Number | K812610 |
| Device Name: | SIEMENS-ELEMA PULSE GENERATOR 668 B |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | SIEMENS CORP. 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 | 1981-09-15 |
| Decision Date | 1981-12-10 |