The following data is part of a premarket notification filed by Telectronics, Inc. with the FDA for Electrode Leads 030-267 & 030-268.
| Device ID | K832110 |
| 510k Number | K832110 |
| Device Name: | ELECTRODE LEADS 030-267 & 030-268 |
| Classification | Permanent Pacemaker Electrode |
| Applicant | TELECTRONICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTB |
| CFR Regulation Number | 870.3680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-30 |
| Decision Date | 1983-08-12 |