510(k) K052783 ยท DQX Wire, Guide, Catheter
MODIFICATION TO: IQ GUIDE WIRE, MODELS 38950-XX. 38951-XX
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 27, 2005 |
| Received | Oct 3, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052783
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.