510(k) K093882
K093882 is an FDA 510(k) premarket notification submitted by Sorin Group Deutschland GmbH for the device "SORIN C5 SYSTEM MODEL 58-00-00". The FDA issued a decision of Substantially Equivalent on January 15, 2010. 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
- January 15, 2010
- Date Received
- December 18, 2009
- 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