K-number	K883779
Device name	WALLABY(TM) BLANKET
Applicant	Fiberoptic Medical Products, Inc.
Product code	LBI
Device class	Class II
Decision date	Nov 14, 1988
Decision	Substantially Equivalent
Regulation	880.5700

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View the full FDA submission: accessdata.fda.gov

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WALLABY(TM) BLANKET

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