K-number	K801539
Device name	ASSURE LEVEL II PROD. #30172
Applicant	Warner-Lambert Co.
Product code	JJY
Device class	Class I
Decision date	Sep 9, 1980
Decision	Substantially Equivalent
Regulation	862.1660

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View the full FDA submission: accessdata.fda.gov

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ASSURE LEVEL II PROD. #30172

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