510(k) K093636 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
STERLING ES MONORAIL AND OVER-THE-WIRE PTA BALLOON DILATATION CATHETERS MODEL H74939334XXXXXXX
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Dec 23, 2009 |
| Received | Nov 24, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093636
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.