K-number	K032469
Device name	AESKULISA ANA 8PRO
Applicant	Aesku, Inc.
Product code	LLL
Device class	Class II
Decision date	Dec 16, 2003
Decision	Substantially Equivalent
Regulation	866.5100

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View the full FDA submission: accessdata.fda.gov

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AESKULISA ANA 8PRO

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