510(k) K192230 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MF SAFECATH
| Applicant | Medifirst Co., Ltd., Cheonan-Si, KR |
| Decision | Substantially Equivalent, Apr 23, 2020 |
| Received | Aug 16, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192230
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.