510(k) K142258 ยท FDI Snare, Flexible
PolyCatch Retrieval Device
| Applicant | Medi-Globe Corporation, Tempe AZ, US |
| Decision | Substantially Equivalent, Sep 30, 2014 |
| Received | Aug 14, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142258
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.