K-number	K970991
Device name	DATEX ENGSTOM MANUAL RESUSCITATOR
Applicant	Promedic, Inc.
Product code	BTM
Device class	Class II
Decision date	Jun 16, 1997
Decision	Unknown
Regulation	868.5915

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View the full FDA submission: accessdata.fda.gov

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DATEX ENGSTOM MANUAL RESUSCITATOR

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