510(k) K993052 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
VYGON 2 FR EPICUTANEO PUR-CATHETER
| Applicant | Vygon Corp., West Cadwell NJ, US |
| Decision | Substantially Equivalent, Aug 3, 2000 |
| Received | Sep 13, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993052
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.