510(k) K071145 ยท MPB Catheter, Hemodialysis, Non-Implanted
NIPRO SAFETOUCH TULIP SAFETY FISTULA NEEDLE
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, Sep 7, 2007 |
| Received | Apr 24, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K071145
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 23, 2015 | Nipro Medical Corporation Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring an extracorporeal circuit of larger volumes of blo Terminated |
LLB | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.