K-number	K801244
Device name	ROCHE HCG STANDARDS
Applicant	Hoffmann-La Roche, Inc.
Product code	JHI
Device class	Class II
Decision date	Jun 20, 1980
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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ROCHE HCG STANDARDS

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