510(k) K881052 ยท FPA Set, Administration, Intravascular
CHECK VALVE
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, May 26, 1988 |
| Received | Mar 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881052
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 21, 2003 | Baxter Healthcare Corp. Interlink System Solution Set with Microbore Tubing, 60 Drops/mL, 123'', 2 injection sites, Male Luer Lock Adapter, catalog 2C6426; Baxter Healthcare Corporation, Deerfield, IL 60015 USA Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.