510(k) K151638 ยท DQY Catheter, Percutaneous
Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter
| Applicant | Cathera, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Nov 13, 2015 |
| Received | Jun 17, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151638
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.