K-number	K123478
Device name	STINGRAY BIPOLAR FORCEPS
Applicant	Stingray Surgical Products
Product code	GEI
Device class	Class II
Decision date	May 10, 2013
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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STINGRAY BIPOLAR FORCEPS

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