510(k) K000570 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BLUE MAX BALLOON DILATATION CATHETER, MAXFORCE BALLOON CATHETER, XXL BALLOON DILATATION CATHATER, SYMMETRY BALLOON DILA
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Apr 13, 2000 |
| Received | Feb 22, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000570
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.