510(k) K914210 ยท FKA Dilator, Vessel
VAS-CATH DUALATOR(TM) VESSEL DILATOR
| Applicant | Vas-Cath, Inc., Mississauga, Ontario, CA |
| Decision | Substantially Equivalent, Jul 1, 1993 |
| Received | Sep 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914210
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.