510(k) K201652 ยท MJN Catheter, Intravascular Occluding, Temporary
COBRA-OS Kit
| Applicant | Front Line Medical Technologies, Inc., London, CA |
| Decision | Unknown, Feb 22, 2021 |
| Received | Jun 18, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201652
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.