510(k) K820648 ยท DQY Catheter, Percutaneous
ARROW M.I.S. MULTI-LUMEN CATHETERIZA
| Applicant | Arrow Intl., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 14, 1982 |
| Received | Mar 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820648
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 11, 2018 | Arrow International Inc 4Fr. Catheter Clamp with Fastener; Product Code: CC-00004 Terminated |
DQY | None listed |
| Apr 11, 2018 | Arrow International Inc 5Fr. Catheter Clamp with Fastener; Product Code: CC-00005 Terminated |
DQY | None listed |
| Apr 11, 2018 | Arrow International Inc 7Fr. Catheter Clamp with Fastener; Product Code: CC-00007 Terminated |
DQY | None listed |
| Apr 11, 2018 | Arrow International Inc 8Fr. Catheter Clamp with Fastener; Product Code: CC-00008 Terminated |
DQY | None listed |
| Sep 25, 2010 | Arrow International Inc Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features) Terminated |
DQY | None listed |
| Sep 25, 2010 | Arrow International Inc Multi-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features) Terminated |
DQY | None listed |
| Sep 25, 2010 | Arrow International Inc Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue Catheter Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.