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U.S. Department of Health and Human Services

Product Classification

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Device apparatus, autotransfusion
Regulation Description Autotransfusion apparatus.
Regulation Medical Specialty Anesthesiology
Review Panel Anesthesiology
Product CodeCAC
Premarket Review Center for Biologics Evaluation & Research (CBER)
Submission Type 510(k)
Regulation Number 868.5830
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Third Party Review Not Third Party Eligible
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