510(k) K051670 ยท PDU Catheter For Crossing Total Occlusions
RF TUNNELER WIRE
| Applicant | Baylis Medical Co., Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Mar 30, 2006 |
| Received | Jun 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051670
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.