510(k) K771764

CORONARY PRESSURE PERFUSION PUMP by 3M Health Care, Sarns — Product Code DXS

K771764 is an FDA 510(k) premarket notification submitted by 3M Health Care, Sarns for the device "CORONARY PRESSURE PERFUSION PUMP". The FDA issued a decision of Substantially Equivalent on September 30, 1977. The device falls under product code DXS (Gauge, Pressure, Coronary, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4310. 3M Health Care, Sarns has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 1977
Date Received
September 19, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauge, Pressure, Coronary, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4310
Review Panel
CV
Submission Type