510(k) K070502 ยท DQY Catheter, Percutaneous
RADIUS SNARE
| Applicant | Radius Medical Technologies, Inc., Acton MA, US |
| Decision | Substantially Equivalent, Oct 4, 2007 |
| Received | Feb 21, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070502
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.