K-number	K123319
Device name	GYRUS ACMI BICOAG HEMOSTASIS PROBE
Applicant	Olympus Surgical Technologies America
Product code	KNS
Device class	Class II
Decision date	Dec 14, 2012
Decision	Substantially Equivalent
Regulation	876.4300

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Source

View the full FDA submission: accessdata.fda.gov

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GYRUS ACMI BICOAG HEMOSTASIS PROBE

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