510(k) K760403 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
TEMPORARY ATRIAL ELECTRODE KIT
| Applicant | Usci, Div. C.R. Bard, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 23, 1976 |
| Received | Aug 9, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760403
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.