510(k) K220934 ยท MOF Guide, Wire, Catheter, Neurovasculature
RADIFOCUS Torque Device
| Applicant | Terumo Medical Products (Hangzhou) Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Jun 29, 2022 |
| Received | Mar 31, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220934
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.