510(k) K081936

SOLEX CATHETER, MODEL SL2593 by Alsius Corp. — Product Code NCX

K081936 is an FDA 510(k) premarket notification submitted by Alsius Corp. for the device "SOLEX CATHETER, MODEL SL2593". The FDA issued a decision of Substantially Equivalent on August 13, 2008. 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
SESE (Substantially Equivalent)
Decision Date
August 13, 2008
Date Received
July 7, 2008
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