510(k) K071358
K071358 is an FDA 510(k) premarket notification submitted by Radiant Medical for the device "REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM". The FDA issued a decision of Substantially Equivalent on June 1, 2007. The device falls under product code NCX (System, Hypothermia, Intravenous, Cooling), a Class II device regulated under 21 CFR 870.5900. Radiant Medical has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 1, 2007
- Date Received
- May 15, 2007
- 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