510(k) K151896 ยท DQY Catheter, Percutaneous
Houdini Catheter
| Applicant | Cruzar Medsystems, Inc., Braintree MA, US |
| Decision | Substantially Equivalent, Dec 7, 2015 |
| Received | Jul 10, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151896
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.