510(k) K252398 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
SURFLO Hybria Closed System Safety IV Catheter
| Applicant | Terumo Medical Products (Hangzhou) Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Dec 17, 2025 |
| Received | Jul 31, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252398
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.