510(k) K071358

REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM by Radiant Medical — Product Code NCX

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