510(k) K913689 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SUB-4(TM), PERIPHERAL DILATATION CATHETER
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Oct 16, 1991 |
| Received | Aug 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913689
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.