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510(k) K222297

CentriMag Pre-connected Pack by Abbott — Product Code DTZ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 1, 2022
Date Received
August 1, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Oxygenator, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4350
Review Panel
CV
Submission Type

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