The following data is part of a premarket notification filed by Oscor Inc. with the FDA for Leads, Implantable Cardiac Pacemakers.
| Device ID | K782018 |
| 510k Number | K782018 |
| Device Name: | LEADS, IMPLANTABLE CARDIAC PACEMAKERS |
| Classification | Permanent Pacemaker Electrode |
| Applicant | Oscor Inc. 3816 DeSoto Blvd. Palm Harbor, FL 34683 |
| Product Code | DTB |
| CFR Regulation Number | 870.3680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-12-05 |
| Decision Date | 1979-06-04 |