K-number	K993321
Device name	R&D HGB/GLC WHOLE BLOOD CONTROL
Applicant	R&D Systems, Inc.
Product code	GGM
Device class	Class II
Decision date	Nov 12, 1999
Decision	Substantially Equivalent
Regulation	864.8625

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View the full FDA submission: accessdata.fda.gov

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R&D HGB/GLC WHOLE BLOOD CONTROL

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