510(k) K031123
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 14, 2003
- Date Received
- April 9, 2003
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Ventricular
- Device Class
- Class II
- Regulation Number
- 882.4100
- Review Panel
- NE
- Submission Type