K-number	K912067
Device name	POLARIS, GYNECOLOGY INDICATIONS
Applicant	Pfizer Laser Systems
Product code	GEX
Device class	Class II
Decision date	Jun 16, 1992
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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POLARIS, GYNECOLOGY INDICATIONS

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