ClearanceBrief
510(k) K970180 ยท LLN Device, Vibration Threshold Measurement

VSA 3000 VIBRATORYN SENSORY ANALYZER

ApplicantEare Consulting Service, Eilat, IL
DecisionSubstantially Equivalent, Apr 25, 1997
ReceivedJan 17, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970180

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.