510(k) K210602 ยท MJN Catheter, Intravascular Occluding, Temporary
AortaSTAT Occlusion Device
| Applicant | Renalpro Medical, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 9, 2021 |
| Received | Mar 1, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210602
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.