510(k) K960281 ยท DTB Permanent Pacemaker Electrode
IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORY
| Applicant | Intermedics, Inc., Angleton TX, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jun 18, 1996 |
| Received | Jan 19, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960281
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.