K-number	K990010
Device name	ALTHIN MEDICAL AB ALTRACART II
Applicant	Althin Medical AB
Product code	KPO
Device class	Class II
Decision date	Apr 15, 1999
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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ALTHIN MEDICAL AB ALTRACART II

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