510(k) K020430 ยท NFK Kit, Repair, Catheter, Hemodialysis
DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)
| Applicant | Diatek, Inc., Winston-Salem NC, US |
| Decision | Substantially Equivalent, May 9, 2002 |
| Received | Feb 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020430
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 6, 2020 | Arrow International Inc Cannon II Plus Replacement Hub Set - Product Usage: is indicated for use in the replacement of a Cannon II Plus hub connection assembly that has been damaged. Terminated |
NFK | None listed |
| Jul 6, 2020 | Arrow International Inc NextStep Retrograde Replacement Hub Set - Product Usage: is indicated for use in the replacement of a NextStep Retrograde hub connection assembly that has been damaged. Terminated |
NFK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.