K-number	K010724
Device name	SOLA 700,SOLA 500, SOLA 300
Applicant	Drager Medizintechnik GmbH
Product code	FTD
Device class	Class II
Decision date	Jun 7, 2001
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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SOLA 700,SOLA 500, SOLA 300

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