K-number	K092090
Device name	ERBELIFT HAND PUMP AND FLEXIBLE PROBE
Applicant	Byrne Medical, Inc.
Product code	FBK
Device class	Class II
Decision date	Nov 30, 2009
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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ERBELIFT HAND PUMP AND FLEXIBLE PROBE

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