510(k) K022321
K022321 is an FDA 510(k) premarket notification submitted by Stockert Instrumente GmbH for the device "STOCKERT V172-28 VENOUS FEMORAL CANNULA". The FDA issued a decision of Substantially Equivalent on October 9, 2002. The device falls under product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4210. Stockert Instrumente GmbH has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 9, 2002
- Date Received
- July 17, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4210
- Review Panel
- CV
- Submission Type