K-number	K081179
Device name	MAMMOSITE CAVITY EVALUATION DEVICE
Applicant	Hologic, Inc.
Product code	JAQ
Device class	Class II
Decision date	May 9, 2008
Decision	Substantially Equivalent
Regulation	892.5700

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View the full FDA submission: accessdata.fda.gov

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MAMMOSITE CAVITY EVALUATION DEVICE

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