510(k) K932301 ยท FPB Filter, Infusion Line
FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Nov 10, 1993 |
| Received | May 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932301
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 11, 2012 | Baxter Healthcare Corp. Baxter Interlink System Straight Type Blood Set with 40 and 150 Micron Dual Screen Filter, Length 86" (2.2 m), Injection Site, Male Luer Lock Adapter; an Rx sterile, nonpyrogenic fluid pathway for the Terminated |
FPA | None listed |
| Jan 11, 2012 | Baxter Healthcare Corp. Baxter Interlink System Y-Type Blood/Solution Set with 40 and 150 Micron Dual Screen Filter, Length 95" (2.4 m), Injection Site, Male Luer Lock Adapter; an Rx sterile, nonpyrogenic fluid pathway for t Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.