510(k) K953017 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
LOW PROFILE TITANIUM MODEL CATALOG #1003
| Applicant | Therex Corp., Walpole MA, US |
| Decision | Substantially Equivalent, Sep 8, 1995 |
| Received | Jun 29, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953017
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.