510(k) K060308
K060308 is an FDA 510(k) premarket notification submitted by Alsius Corp. for the device "COOLGARD 3000". The FDA issued a decision of SESU on April 26, 2006. The device falls under product code NCX (System, Hypothermia, Intravenous, Cooling), a Class II device regulated under 21 CFR 870.5900. Alsius Corp. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESU ()
- Decision Date
- April 26, 2006
- Date Received
- February 7, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Hypothermia, Intravenous, Cooling
- Device Class
- Class II
- Regulation Number
- 870.5900
- Review Panel
- NE
- Submission Type