510(k) K910924 ยท DTB Permanent Pacemaker Electrode
ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONE
| Applicant | Pacesetter Systems, Sylmar CA, US |
| Decision | Substantially Equivalent, Aug 28, 1991 |
| Received | Mar 5, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910924
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.