510(k) K952537 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
THEREX LOW PROFILE TITANIUM MODEL 1.0MM I.D./1.8MM O.D.
| Applicant | Therex Corp., Walpole MA, US |
| Decision | Substantially Equivalent, Jul 6, 1995 |
| Received | May 31, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952537
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.