510(k) K872472 ยท DXT Injector And Syringe, Angiographic
SCHNEIDER-SHILEY BIFLATOR BALLOON INFLATION DEVICE
| Applicant | Angiomedics, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 14, 1987 |
| Received | Jun 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872472
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.