K-number	K963349
Device name	DEVILBISS 8650D
Applicant	Devilbiss Health Care, Inc.
Product code	BTI
Device class	Class II
Decision date	Jun 13, 1997
Decision	Substantially Equivalent
Regulation	868.6250

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View the full FDA submission: accessdata.fda.gov

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DEVILBISS 8650D

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