510(k) K981792 ยท FPA Set, Administration, Intravascular
SOLUTION ADMINISTRATION SET
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Aug 17, 1998 |
| Received | May 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981792
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 14, 2007 | Baxter Healthcare Corp. Baxter Clearlink System Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubing, non-DEHP 12 inch pump segment, 0.22 micron downstream high pressure filter, Luer activated valve, Terminated |
FPA | None listed |
| Mar 14, 2007 | Baxter Healthcare Corp. Baxter Interlink System Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubing, non-DEHP pump segment, 0.22 micron downstream high pressure filter, injection site, male Luer loc Terminated |
FPA | None listed |
| Mar 14, 2007 | Baxter Healthcare Corp. Baxter Vented Paclitaxel Set; a sterile fluid pathway with polyethylene lined tubing, non-DEHP pump segment, 0.22 micron downstream high pressure filter, injection site, male Luer lock adapter; for us Terminated |
FPA | None listed |
| Nov 16, 2004 | Baxter Healthcare Corp. Baxter Clearlink Intravenous (IV) Delivery System; the system consists of solution sets, extension sets and blood sets that have a luer activated valve for IV access, which allows the administration Terminated |
FPA | None listed |
| Aug 21, 2003 | Baxter Healthcare Corp. Clearlink System Vented Paclitaxel Set, 10 drops/mL, 111'', Polyethylene Lined Tubing, Non-DEHP Pump Segment, 0.22 Micron Extended Life Filter, Luer Activated Valve, Male Luer Lock Adapter, catalog 2C Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.