510(k) K820729

SARNS PULSATILE PUMP by 3M Health Care, Sarns — Product Code DWB

K820729 is an FDA 510(k) premarket notification submitted by 3M Health Care, Sarns for the device "SARNS PULSATILE PUMP". The FDA issued a decision of Substantially Equivalent on November 1, 1982. The device falls under product code DWB (Pump, Blood, Cardiopulmonary Bypass, Roller Type), a Class II device regulated under 21 CFR 870.4370. 3M Health Care, Sarns has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 1, 1982
Date Received
March 17, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Blood, Cardiopulmonary Bypass, Roller Type
Device Class
Class II
Regulation Number
870.4370
Review Panel
CV
Submission Type