510(k) K881743 ยท LFJ Catheter, Subclavian
VAS-CATH FLEXXICON DUAL LUMEN DIALYSIS CATHETER
| Applicant | Vas-Cath, Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Jun 23, 1988 |
| Received | Apr 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881743
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.