K-number	K023793
Device name	1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
Applicant	Portex, Inc.
Product code	BTM
Device class	Class II
Decision date	Feb 11, 2003
Decision	Substantially Equivalent
Regulation	868.5915

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View the full FDA submission: accessdata.fda.gov

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1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR

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