510(k) K934191 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
NEW BLUE MAX BALLOON DILATATION CATHETER
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Dec 9, 1993 |
| Received | Aug 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934191
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.