510(k) K914121 ยท DTB Permanent Pacemaker Electrode
VASCOSCREW 6/60 AND VASCOSCREW 8/60
| Applicant | Vascor Medical Corp., Tarpon Springs FL, US |
| Decision | Substantially Equivalent, Aug 24, 1993 |
| Received | Sep 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914121
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.