K-number	K823247
Device name	U-WAY QUICKOLLAR
Applicant	Ems Industries, Inc.
Product code	IQK
Device class	Class I
Decision date	Nov 16, 1982
Decision	Substantially Equivalent
Regulation	890.3490

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Source

View the full FDA submission: accessdata.fda.gov

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U-WAY QUICKOLLAR

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