K-number	K880890
Device name	THE S.A.F.E. SYSTEM
Applicant	Pfizer Laser Systems
Product code	FYD
Device class	Class II
Decision date	May 11, 1988
Decision	Substantially Equivalent
Regulation	878.5070

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View the full FDA submission: accessdata.fda.gov

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THE S.A.F.E. SYSTEM

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