ClearanceBrief
510(k) K761219 ยท KIE Apparatus, High Pressure Liquid Chromatography

SERIES II LIQUID CHROMATOGRAPH

ApplicantThe Perkin-Elmer Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 1, 1977
ReceivedDec 7, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K761219

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.