K-number	K092368
Device name	REPROCESSED PULSE OXIMETER SENSORS
Applicant	Sterilmed, Inc.
Product code	NLF
Device class	Class II
Decision date	Nov 3, 2009
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED PULSE OXIMETER SENSORS

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