510(k) K934787 ยท LDF Electrode, Pacemaker, Temporary
SILICORE SEMI-FLOATER
| Applicant | Electro-Catheter Corp., Rahway NJ, US |
| Decision | Substantially Equivalent, Feb 24, 1995 |
| Received | Oct 5, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934787
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.