K-number	K955434
Device name	ACCESS FOLATE ASSAY (MODIFICATION)
Applicant	Beckman Coulter, Inc.
Product code	CGN
Device class	Class II
Decision date	Jan 29, 1996
Decision	Substantially Equivalent
Regulation	862.1295

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Source

View the full FDA submission: accessdata.fda.gov

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ACCESS FOLATE ASSAY (MODIFICATION)

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