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510(k) K960392

CDM by Bio-Rad — Product Code LDM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 8, 1996
Date Received
January 29, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrumentation, High Pressure Liquid Chromatography
Device Class
Class I
Regulation Number
862.2260
Review Panel
TX
Submission Type

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