K-number	K974488
Device name	AIRPREP SYSTEM - MODEL 9001
Applicant	Asi Medical, Inc.
Product code	KOJ
Device class	Class II
Decision date	May 26, 1998
Decision	Substantially Equivalent
Regulation	872.6080

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View the full FDA submission: accessdata.fda.gov

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AIRPREP SYSTEM - MODEL 9001

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