510(k) K200459 ยท MJN Catheter, Intravascular Occluding, Temporary
pREBOA-PRO Catheter
| Applicant | Prytime Medical Devices, Inc., Boerne TX, US |
| Decision | Substantially Equivalent, Jun 3, 2020 |
| Received | Feb 25, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200459
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.