510(k) K244059 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen Midline Catheter - Max Barrier Kit (70006104); HydroMID 5F Dual Lumen Midline Catheter - Mobile Max Barrier Kit (90006104)
| Applicant | Access Vascular, Inc., Billerica MD, US |
| Decision | Substantially Equivalent, Mar 27, 2025 |
| Received | Dec 31, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K244059
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.