K-number	K913900
Device name	V*CARE MANUAL RESUSCITATOR, CAT#VR-1000
Applicant	Ventlab Corp.
Product code	BTM
Device class	Class II
Decision date	Jan 7, 1992
Decision	Substantially Equivalent
Regulation	868.5915

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View the full FDA submission: accessdata.fda.gov

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V*CARE MANUAL RESUSCITATOR, CAT#VR-1000

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