K-number	K962320
Device name	S3 CARDIOPLEGIA CONTROL
Applicant	Stoeckert Instrumente
Product code	DTR
Device class	Class II
Decision date	Jan 10, 1997
Decision	Substantially Equivalent
Regulation	870.4240

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View the full FDA submission: accessdata.fda.gov

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S3 CARDIOPLEGIA CONTROL

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