ClearanceBrief
510(k) K811966 ยท FMI Needle, Hypodermic, Single Lumen

VISITEC NEEDLE RANGE (GENERAL HOSPITAL)

ApplicantVisitec Co., Walker MI, US
DecisionSubstantially Equivalent, Jul 23, 1981
ReceivedJul 10, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811966

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.