510(k) K993387 ยท FRN Pump, Infusion
IPUMP PAIN MANAGEMENT SYSTEM, MODEL 2L3107K
| Applicant | Baxter Healthcare Corp, Round Lake IL, US |
| Decision | Substantially Equivalent, Nov 1, 1999 |
| Received | Oct 8, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K993387
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 26, 2006 | Baxter Healthcare Corp. Baxter I-Pump Pain Management System infusion pump, product codes 2L3107, 2L3107K and 2L3107R, Baxter Healthcare Corporation, Deerfield, IL 60015 Terminated |
MEA | None listed |
| Apr 26, 2006 | Baxter Healthcare Corp. Baxter I-Pump Pain Management System infusion pump, product codes 2L3107, 2L3107K and 2L3107R, Baxter Healthcare Corporation, Deerfield, IL 60015 Terminated |
MEA | None listed |
| Nov 16, 2005 | Baxter Healthcare Corp. Baxter I-Pump Pain Management System infusion pump, product codes 2L3107, 2L3107K and 2L3107R, Baxter Healthcare Corporation, Deerfield, IL 60015 Terminated |
FRN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.