K-number	K850200
Device name	SUCTION REGULATOR 7700 SERIES
Applicant	Boehringer Laboratories
Product code	KDP
Device class	Class II
Decision date	Mar 4, 1985
Decision	Substantially Equivalent
Regulation	880.6740

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View the full FDA submission: accessdata.fda.gov

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SUCTION REGULATOR 7700 SERIES

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