K-number	K042077
Device name	BITECH BIPOLAR SCISSORS
Applicant	Guenter Bissinger Medizintechnik GmbH
Product code	GEI
Device class	Class II
Decision date	Oct 27, 2004
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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BITECH BIPOLAR SCISSORS

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