K-number	K800047
Device name	LDC UVIII FIXED WAVELENGTH ULTRAVIOLET
Applicant	Laboratory Data Control
Product code	KIE
Device class	Class I
Decision date	Jan 21, 1980
Decision	Substantially Equivalent
Regulation	862.2260

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View the full FDA submission: accessdata.fda.gov

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LDC UVIII FIXED WAVELENGTH ULTRAVIOLET

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