K-number	K901559
Device name	MODIFICATION TO API UNISCEPT 20GP
Applicant	Analytical Products, Inc.
Product code	LQL
Device class	Class I
Decision date	Sep 10, 1990
Decision	Substantially Equivalent
Regulation	866.2660

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO API UNISCEPT 20GP

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