K-number	K920134
Device name	PHILIPS 41 SERIES RAINBOW
Applicant	Philips Int'L B.V.
Product code	ESD
Device class	Class I
Decision date	Jan 24, 1992
Decision	Substantially Equivalent
Regulation	874.3300

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Source

View the full FDA submission: accessdata.fda.gov

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PHILIPS 41 SERIES RAINBOW

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