K-number	K812022
Device name	ZEE MANUAL RESUSCITATOR
Applicant	Zee Medical Products Co., Inc.
Product code	BTM
Device class	Class II
Decision date	Jul 31, 1981
Decision	Substantially Equivalent
Regulation	868.5915

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View the full FDA submission: accessdata.fda.gov

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ZEE MANUAL RESUSCITATOR

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