510(k) K900605 ยท DTD Pacemaker Lead Adaptor
3.2-5MM UNIPOLAR LEAD UPSIZING KIT, MODEL AK 100
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 6, 1990 |
| Received | Feb 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900605
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.