510(k) K192135 ยท DQY Catheter, Percutaneous
VIA Microcatheter (size 17), VIA Microcatheter (size 21), VIA Microcatheter (size 27), VIA Microcatheter (size 33)
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Dec 24, 2019 |
| Received | Aug 7, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192135
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 21, 2021 | MICROVENTION INC. VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature. Terminated |
DQY | None listed |
| Apr 21, 2021 | MICROVENTION INC. VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature. Terminated |
DQY | None listed |
| Apr 21, 2021 | MICROVENTION INC. VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature. Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.