510(k) K021441 ยท MMX Device, Percutaneous Retrieval
RADIUS SNARE
| Applicant | Radius Medical Technologies, Inc., Maynard MA, US |
| Decision | Substantially Equivalent, Jun 14, 2002 |
| Received | May 6, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021441
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.