K-number	K781581
Device name	SURGICAL LIGHT 22 SERIES
Applicant	American Sterilizer Co.
Product code	FQP
Device class	Class II
Decision date	Oct 17, 1978
Decision	Substantially Equivalent
Regulation	878.4580

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Source

View the full FDA submission: accessdata.fda.gov

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SURGICAL LIGHT 22 SERIES

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