K-number	K092554
Device name	BLASTOMERE BIOPSY PIPETTES, POLAR BODY BIOPSY PIPETTES
Applicant	Sunlight Medical, Inc.
Product code	MQH
Device class	Class II
Decision date	Apr 30, 2010
Decision	Substantially Equivalent
Regulation	884.6130

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View the full FDA submission: accessdata.fda.gov

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BLASTOMERE BIOPSY PIPETTES, POLAR BODY BIOPSY PIPETTES

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