510(k) K861714

STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE by Shiley, Inc. — Product Code DWB

K861714 is an FDA 510(k) premarket notification submitted by Shiley, Inc. for the device "STOCKERT-SHILEY MULTIFLOW ROLLER PUMP MODULE". The FDA issued a decision of Substantially Equivalent on July 16, 1986. The device falls under product code DWB (Pump, Blood, Cardiopulmonary Bypass, Roller Type), a Class II device regulated under 21 CFR 870.4370. Shiley, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 16, 1986
Date Received
May 5, 1986
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