510(k) K926011 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
A-PORT IMPLANT VASCU ACCESS SYST PROD LIN EXT-MODI
| Applicant | Therex Corp., Walpole MA, US |
| Decision | Substantially Equivalent, Mar 19, 1993 |
| Received | Nov 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926011
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 19, 2006 | Arrow International Inc Implantable Vascular Access system --Infusion Ports with Silicone Rubber Catheter.
Latex-free A Port. 9 Fr. Introducer Kit.
Ref. Product No. AP-06018. Terminated |
LJT | None listed |
| Dec 19, 2006 | Arrow International Inc Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter.
Latex-Free A Port. 6 Fr. Introducer Kit.
Ref Product No. AP-06014 Terminated |
LJT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.