510(k) K842113 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
AMENDMENT TO ANGIOGRAPHY KIT W/ADDIT
| Applicant | Mallinckrodt Critical Care, Walker MI, US |
| Decision | Substantially Equivalent, Jul 13, 1984 |
| Received | Mar 19, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842113
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.