K-number	K942311
Device name	DYNASTY U1-33 AGM
Applicant	Foley & Lardner
Product code	KNN
Device class	Class I
Decision date	Nov 7, 1994
Decision	Substantially Equivalent
Regulation	890.3920

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View the full FDA submission: accessdata.fda.gov

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DYNASTY U1-33 AGM

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