510(k) K100351 ยท DQX Wire, Guide, Catheter
NEUROSCOUT STEERABLE GUIDEWIRE
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Mar 16, 2010 |
| Received | Feb 12, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100351
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.