510(k) K133681 ยท MMX Device, Percutaneous Retrieval
CRUX SNARE FILTER RETRIEVAL SET
| Applicant | Volcano Corporation, Billerica MA, US |
| Decision | Substantially Equivalent, Jan 30, 2014 |
| Received | Dec 2, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133681
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.