510(k) K111252 ยท DQY Catheter, Percutaneous
ACUITY (TM) CUT-AWAY (TM) GUIDE CATHETERS 6F AND 8F
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 2, 2011 |
| Received | May 3, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111252
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.