510(k) K933350 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
THEREX LOW-PROFILE PORT 1.5MM I.D. X 2.7MM O.D. DETACHED CATHETER SYSTEM
| Applicant | Therex Corp., Walpole MA, US |
| Decision | Unknown, Feb 23, 1994 |
| Received | Jul 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933350
| 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 Low Profile Port. 9 Fr. Introducer Kit
Ref Product No. AP-06020 Terminated |
LJT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.