K-number	K101561
Device name	TX1 TISSUE REMOVAL SYSTEM
Applicant	American Optisurgical, Inc.
Product code	LFL
Device class	Class U
Decision date	Aug 27, 2010
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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TX1 TISSUE REMOVAL SYSTEM

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