510(k) K093977 ยท DQY Catheter, Percutaneous
ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX
| Applicant | Chestnut Medical Technologies, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Apr 22, 2010 |
| Received | Dec 24, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093977
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.