510(k) K951098 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
HDC VADD (VASCULAR ACCESS DEVICE) TUNNELER
| Applicant | Hdc Corp., San Jose CA, US |
| Decision | Substantially Equivalent, Jun 2, 1995 |
| Received | Mar 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951098
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.