K-number	K030864
Device name	VADI MANUAL RESUSCITATOR
Applicant	Vedi Corp.
Product code	BTM
Device class	Class II
Decision date	Jan 30, 2004
Decision	Substantially Equivalent
Regulation	868.5915

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Source

View the full FDA submission: accessdata.fda.gov

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VADI MANUAL RESUSCITATOR

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