ClearanceBrief
510(k) K800046 ยท KIE Apparatus, High Pressure Liquid Chromatography

LDC CHROMATOGRAPHY ACCESSORY MODULE B

ApplicantLaboratory Data Control, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 25, 1980
ReceivedJan 9, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800046

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.