510(k) K193569 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
PIVO(TM)
| Applicant | Velano Vascular, San Francisco CA, US |
| Decision | Substantially Equivalent, Jan 21, 2020 |
| Received | Dec 23, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K193569
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 10, 2021 | Velano Vascular PIVO Blood Collection Device 20G, REF: 202-0005 Terminated |
JKA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.