510(k) K151821 ยท DQY Catheter, Percutaneous
ER-REBOA Catheter
| Applicant | Pryor Medical Devices, Inc., Boeme TX, US |
| Decision | Substantially Equivalent, Oct 23, 2015 |
| Received | Jul 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151821
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.