K-number	K991183
Device name	DORNIER LASERTRODE FIBER
Applicant	Dornier Surgical Products, Inc.
Product code	GEX
Device class	Class II
Decision date	Jun 9, 1999
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DORNIER LASERTRODE FIBER

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