510(k) K896568 ยท LFJ Catheter, Subclavian
DUALYSE-CATH - CODES #1132.212, 1132.112
| Applicant | Vygon Corp., New York NY, US |
| Decision | Substantially Equivalent, May 9, 1990 |
| Received | Nov 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896568
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.