510(k) K071318

MODIFICATION TO: STOCKERT S5 SYSTEM by Sorin Group Deutschland GmbH — Product Code DTQ

K071318 is an FDA 510(k) premarket notification submitted by Sorin Group Deutschland GmbH for the device "MODIFICATION TO: STOCKERT S5 SYSTEM". The FDA issued a decision of Substantially Equivalent on July 6, 2007. The device falls under product code DTQ (Console, Heart-Lung Machine, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4220. Sorin Group Deutschland GmbH has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 6, 2007
Date Received
May 10, 2007
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Console, Heart-Lung Machine, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4220
Review Panel
CV
Submission Type