K-number	K915863
Device name	MEGA AMNIOCENTESIS KIT
Applicant	Mega Medical, Inc.
Product code	HIO
Device class	Class I
Decision date	Mar 30, 1992
Decision	Substantially Equivalent — Kit Device
Regulation	884.1550

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View the full FDA submission: accessdata.fda.gov

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MEGA AMNIOCENTESIS KIT

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