K-number	K945914
Device name	BIPOLAR GENERATOR MODEL 2352
Applicant	Richard Wolf Medical Instruments Corp.
Product code	GEI
Device class	Class II
Decision date	Sep 26, 1995
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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BIPOLAR GENERATOR MODEL 2352

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