K-number	K072026
Device name	RNK ELECTRONIC STETHOSCOPE
Applicant	Rnk Products, Inc.
Product code	DQD
Device class	Class II
Decision date	Oct 26, 2007
Decision	Substantially Equivalent
Regulation	870.1875

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View the full FDA submission: accessdata.fda.gov

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RNK ELECTRONIC STETHOSCOPE

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