510(k) K952063 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
XXL BALLON DILATATION CATHETER
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Nov 14, 1995 |
| Received | May 2, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952063
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.