K-number	K831744
Device name	TRANSCUTANEOUS OXYGEN MONITOR OPTION
Applicant	Ge Medical Systems Information Technologies
Product code	KLK
Device class	Class II
Decision date	Jul 19, 1983
Decision	Substantially Equivalent
Regulation	868.2500

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View the full FDA submission: accessdata.fda.gov

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TRANSCUTANEOUS OXYGEN MONITOR OPTION

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