K-number	K151639
Device name	ABL80 FLEX and ABL80 FLEX CO-OX
Applicant	Sendx Medical, Inc.
Product code	CGA
Device class	Class II
Decision date	Dec 7, 2015
Decision	Substantially Equivalent
Regulation	862.1345

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Source

View the full FDA submission: accessdata.fda.gov

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ABL80 FLEX and ABL80 FLEX CO-OX

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