510(k) K915337

CAPIOX LEVEL ALARM by Terumo Medical Corp. — Product Code DTW

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 21, 1992
Date Received
November 26, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4340
Review Panel
CV
Submission Type