510(k) K122772 ยท DQY Catheter, Percutaneous
PENUMBRA DDC CATHETERS
| Applicant | Penumbra, Inc., Alameda CA, US |
| Decision | Substantially Equivalent, Nov 20, 2012 |
| Received | Sep 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122772
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.