K-number	K871932
Device name	MODEL 5050 SURGILASER FOR UROLOGY USE
Applicant	Lasermatic, Inc.
Product code	LNK
Device class	Class II
Decision date	Mar 25, 1988
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MODEL 5050 SURGILASER FOR UROLOGY USE

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