The following data is part of a premarket notification filed by Daig Corp. with the FDA for Pacemaker, Electrode, Perm. & Temp..
| Device ID | K800351 |
| 510k Number | K800351 |
| Device Name: | PACEMAKER, ELECTRODE, PERM. & TEMP. |
| Classification | Permanent Pacemaker Electrode |
| Applicant | DAIG CORP. 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 | 1980-02-15 |
| Decision Date | 1980-05-28 |