510(k) K932671 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
THEREX R-PORT
| Applicant | Therex Corp., Walpole MA, US |
| Decision | Unknown, Feb 7, 1994 |
| Received | Jun 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932671
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.