K-number	K941351
Device name	BURDICK PRO2 OXIMETER
Applicant	Burdick Corp.
Product code	DQA
Device class	Class II
Decision date	Oct 13, 1994
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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BURDICK PRO2 OXIMETER

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