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FDA 510(k) Applications for Medical Device Product Code "LDM"
(Instrumentation, High Pressure Liquid Chromatography)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K960392
BIO-RAD
CDM
07/08/1996
K961557
WATERS CORPORATION
ALLIANCE 2690 SEPARATIONS MODULE
07/05/1996
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