K-number	K150959
Device name	Sutter Bipolar Forceps-Calvian
Applicant	Sutter Medizintechnik GmbH
Product code	GEI
Device class	Class II
Decision date	Sep 10, 2015
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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Sutter Bipolar Forceps-Calvian

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