510(k) K030062 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ADMIRAL .035 DILATATION CATHETER, MODELS ADL0720-80,ADL0720-135,ADL0820-80, ADL0820-135,ADL0920-80,ADL0920-135,ADL1020-0
| Applicant | Avantec Vascular Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Apr 3, 2003 |
| Received | Jan 7, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030062
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.