K-number	K000205
Device name	EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES
Applicant	Rocket Medical Plc
Product code	MQE
Device class	Class II
Decision date	Apr 19, 2000
Decision	Substantially Equivalent
Regulation	884.6100

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View the full FDA submission: accessdata.fda.gov

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EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES

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