K-number	K001315
Device name	MODIFICATION TO KION ANESTHESIA SYSTEM
Applicant	Siemens Elema AB
Product code	BSZ
Device class	Class II
Decision date	May 26, 2000
Decision	Substantially Equivalent
Regulation	868.5160

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO KION ANESTHESIA SYSTEM

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