K-number	K860775
Device name	MEDIASTINAL AUTOTRANSFUSION SYSTEM
Applicant	Cardio Metrics, Inc.
Product code	DTP
Device class	Class II
Decision date	May 28, 1986
Decision	Substantially Equivalent
Regulation	870.4230

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View the full FDA submission: accessdata.fda.gov

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MEDIASTINAL AUTOTRANSFUSION SYSTEM

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