510(k) K050873 ยท DQX Wire, Guide, Catheter
CANALIZER HYDROPHILIC GUIDE WIRE
| Applicant | Medical Device Technologies, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, May 26, 2005 |
| Received | Apr 6, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050873
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.