The following data is part of a premarket notification filed by Telectronics, Inc. with the FDA for Implant Prog Pulse Generator, Unipolar & Bipolar.
| Device ID | K860573 |
| 510k Number | K860573 |
| Device Name: | IMPLANT PROG PULSE GENERATOR, UNIPOLAR & BIPOLAR |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | TELECTRONICS, INC. 40 CRANE HILL RD. Suffield, CT 06078 |
| Contact | W. C Nealon |
| Correspondent | W. C Nealon TELECTRONICS, INC. 40 CRANE HILL RD. Suffield, CT 06078 |
| Product Code | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-02-14 |
| Decision Date | 1986-05-28 |