ClearanceBrief
510(k) K780035 ยท HEL Monitor, Heart Rate, Fetal, Ultrasonic

MINIVISOR

ApplicantMetrix Teknika, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 6, 1978
ReceivedJan 9, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780035

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.