510(k) K921254 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BLUE MAX II BALLOON DDILATATION CATHETER
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Dec 3, 1992 |
| Received | Mar 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921254
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.