510(k) K000210 ยท DTD Pacemaker Lead Adaptor
MODIFICATION TO MODEL 5866-37M LEAD ADAPTOR KIT
| Applicant | Medtronic Vascular, Shoreview MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Feb 23, 2000 |
| Received | Jan 24, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000210
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.