K-number	K864402
Device name	BIPOLAR ELECTROSURGICAL INTRAOCULAR PROBE
Applicant	New England Surgical Instrument Corp.
Product code	GEI
Device class	Class II
Decision date	Jan 20, 1987
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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BIPOLAR ELECTROSURGICAL INTRAOCULAR PROBE

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