510(k) K014109 ยท MMX Device, Percutaneous Retrieval
IN-TIME RETRIEVAL DEVICE
| Applicant | Boston Scientific, Target, Fremont CA, US |
| Decision | Substantially Equivalent, Mar 12, 2002 |
| Received | Dec 14, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014109
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.