510(k) K213002 ยท DYB Introducer, Catheter
SCORPION Portal Vein Access Set
| Applicant | Argon Medical Devices, Athens TX, US |
| Decision | Substantially Equivalent, Oct 14, 2021 |
| Received | Sep 20, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213002
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.