510(k) K003145

ORIGEN BLADDER HOLDER by Origen Biomedical, Inc. — Product Code DWC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 2001
Date Received
October 10, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Controller, Temperature, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4250
Review Panel
CV
Submission Type

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).