510(k) K093822 ยท DQX Wire, Guide, Catheter
DOCKING STATION,TEIRSTEIN EDGE,ANGIOASSIST COMBINATION DEVICE, ANGIOASSIST FAMILY
| Applicant | Shepherd Scientific, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Jan 28, 2010 |
| Received | Dec 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093822
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.