K-number	K122445
Device name	AESPIRE 7900, AESPIRE VIEW
Applicant	Datex-Ohmeda
Product code	BSZ
Device class	Class II
Decision date	Oct 12, 2012
Decision	Substantially Equivalent
Regulation	868.5160

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Source

View the full FDA submission: accessdata.fda.gov

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AESPIRE 7900, AESPIRE VIEW

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