K-number	K760234
Device name	OXIMETER, IN VIVO CATHETER
Applicant	Oximetrix, Inc.
Product code	DQE
Device class	Class II
Decision date	Aug 23, 1976
Decision	Substantially Equivalent
Regulation	870.1230

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View the full FDA submission: accessdata.fda.gov

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OXIMETER, IN VIVO CATHETER

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