The following data is part of a premarket notification filed by Oscor Inc. with the FDA for External Pulse Generator For Temp. Stim.
| Device ID | K831768 |
| 510k Number | K831768 |
| Device Name: | EXTERNAL PULSE GENERATOR FOR TEMP. STIM |
| Classification | Pulse-generator, Pacemaker, External |
| Applicant | Oscor Inc. 3816 DeSoto Blvd. Palm Harbor, FL 34683 |
| Product Code | DTE |
| CFR Regulation Number | 870.3600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-01 |
| Decision Date | 1983-12-16 |