510(k) K220772 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
HydroMID 4F Single Lumen Midline Catheter
| Applicant | Access Vascular, Inc., Ballerica MA, US |
| Decision | Substantially Equivalent, Dec 7, 2022 |
| Received | Mar 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220772
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.