K-number	K800197
Device name	ANAGO DISP., ALL PURPOSE PATIENT REST.
Applicant	Anago, Inc.
Product code	FQM
Device class	Class I
Decision date	Feb 26, 1980
Decision	Substantially Equivalent
Regulation	880.5075

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View the full FDA submission: accessdata.fda.gov

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ANAGO DISP., ALL PURPOSE PATIENT REST.

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