ClearanceBrief
510(k) K761351 ยท KIE Apparatus, High Pressure Liquid Chromatography

L080 SERIES LIQUID CHROMATOGRAPH

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 2, 1977
ReceivedDec 28, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K761351

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.