K-number	K081767
Device name	AMNISURE FETAL MEMBRANES RUPTURE TEST, MODEL FMRT-1
Applicant	Amnisure International, LLC
Product code	NQM
Device class	Class I
Decision date	Jan 9, 2009
Decision	Substantially Equivalent
Regulation	862.1550

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View the full FDA submission: accessdata.fda.gov

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AMNISURE FETAL MEMBRANES RUPTURE TEST, MODEL FMRT-1

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