510(k) K073520 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ANGIOTECH CVC
| Applicant | Angiotech Pharmaceuticals, Inc., Herndon VA, US |
| Decision | Substantially Equivalent, Apr 11, 2008 |
| Received | Dec 14, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073520
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.