K-number	K904766
Device name	DEVILBISS MODEL 7352 SERIES
Applicant	Devilbiss Health Care, Inc.
Product code	BZD
Device class	Class II
Decision date	Mar 26, 1991
Decision	Substantially Equivalent
Regulation	868.5905

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View the full FDA submission: accessdata.fda.gov

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DEVILBISS MODEL 7352 SERIES

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