K-number	K833320
Device name	AMBERLITE CG50 RESIN, 100-200 MESH
Applicant	Biosan Laboratories, Inc.
Product code	KEA
Device class	Class I
Decision date	Dec 8, 1983
Decision	Substantially Equivalent
Regulation	862.2230

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View the full FDA submission: accessdata.fda.gov

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AMBERLITE CG50 RESIN, 100-200 MESH

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