K-number	K822929
Device name	VERIL/PPR PERSONAL PAIN RELIEVER #800
Applicant	Verite
Product code	GZJ
Device class	Class II
Decision date	Nov 17, 1982
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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VERIL/PPR PERSONAL PAIN RELIEVER #800

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