K-number	K801353
Device name	PARKE-DAVIS SURGICAL LIGHT
Applicant	Warner-Lambert Co.
Product code	FTD
Device class	Class II
Decision date	Jun 30, 1980
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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PARKE-DAVIS SURGICAL LIGHT

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