510(k) K882330 ยท LDF Electrode, Pacemaker, Temporary
BARD BAIM-TURI BALLOON DIAGNOSTIC PACING CATHETER
| Applicant | C.R. Bard, Inc., Tewksbury MA, US |
| Decision | Substantially Equivalent, Sep 6, 1988 |
| Received | Jun 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882330
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.