K-number	K020803
Device name	CEFAR MEDICAL AB CEFAR PRIMO
Applicant	Cefar Medical AB
Product code	GZJ
Device class	Class II
Decision date	Jun 10, 2002
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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CEFAR MEDICAL AB CEFAR PRIMO

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