510(k) K853332 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
HDC CHEMO-PORT (VASCULAR)
| Applicant | Hdc Corp., Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 17, 1986 |
| Received | Aug 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853332
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.