510(k) K022201 ยท MMX Device, Percutaneous Retrieval
RADIUS MICRO SNARE
| Applicant | Radius Medical Technologies, Inc., Hopkonton MA, US |
| Decision | Substantially Equivalent, Feb 3, 2003 |
| Received | Jul 5, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022201
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.