510(k) K093970 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
PICA CATHETER
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Jan 15, 2010 |
| Received | Dec 23, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093970
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.