K-number	K954267
Device name	BURDICK 200 PULSE OXIMETER
Applicant	Burdick, Inc.
Product code	DQA
Device class	Class II
Decision date	May 3, 1996
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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BURDICK 200 PULSE OXIMETER

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