510(k) K940651

SARNS ULTRASONIC AIR SENSOR by 3M Health Care, Sarns — Product Code KRL

K940651 is an FDA 510(k) premarket notification submitted by 3M Health Care, Sarns for the device "SARNS ULTRASONIC AIR SENSOR". The FDA issued a decision of Substantially Equivalent on May 24, 1994. The device falls under product code KRL (Detector, Bubble, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4205. 3M Health Care, Sarns has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 24, 1994
Date Received
February 15, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Detector, Bubble, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4205
Review Panel
CV
Submission Type