K-number	K110427
Device name	FEMTEC LASER SYSTEM FOR CAPSULOTOMY
Applicant	Technolas Perfect Vision GmbH
Product code	OOE
Device class	Class II
Decision date	Nov 22, 2011
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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FEMTEC LASER SYSTEM FOR CAPSULOTOMY

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