K-number	K871875
Device name	MODEL 5050 SURGILASER FOR OB-GYN USE
Applicant	Lasermatic, Inc.
Product code	HHR
Device class	Class II
Decision date	Aug 22, 1988
Decision	Substantially Equivalent
Regulation	884.4550

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View the full FDA submission: accessdata.fda.gov

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MODEL 5050 SURGILASER FOR OB-GYN USE

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