510(k) K843261 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
ANGIOSYSTEMS STANDARD ARTERIOGRAM & CARD
| Applicant | Angiosystems, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 11, 1984 |
| Received | Aug 20, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843261
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.