510(k) K032129 ยท DQX Wire, Guide, Catheter
RADIUS 018 COUGAR WIRE
| Applicant | Radius Medical Technologies, Inc., Hopkonton MA, US |
| Decision | Substantially Equivalent, Jul 17, 2003 |
| Received | Jul 10, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032129
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.