510(k) K904334 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
PERCUTANEOUS INTRAVENOUS CATHETER REPAIR KIT
| Applicant | Pharmacia Deltec, Inc., St. Paul MN, US |
| Decision | Unknown, Nov 5, 1990 |
| Received | Sep 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904334
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 30, 2003 | Deltec, Inc Ventra Percutaneous Intravenous Catheter Repair Kit for Luer Connector Segments and Single-Lumen Catheters, Reorder Number 21-0105 Terminated |
FOZ | None listed |
| Jul 30, 2003 | Deltec, Inc Ventra Percutaneous Intravenous Catheter Repair Kit for 9 French Dual-Lumen External Catheter Segment, Reorder Number 21-0106 Terminated |
FOZ | None listed |
| Jul 30, 2003 | Deltec, Inc Ventra Percutaneous Intravenous Catheter Repair Kit for 11 French Triple-Lumen External Catheter Segment, Reorder Number 21-0107 Terminated |
FOZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.