510(k) K811964 ยท DRC Trocar
VISITEC NEEDLE RANGE (CARDIOVASCULAR)
| Applicant | Visitec Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 20, 1981 |
| Received | Jul 10, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811964
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.