Cleared Traditional

K153226 - Solex 7 Intravascular Heat Exchange Catheter, ZOLL Start-Up Kit (FDA 510(k) Clearance)

Mar 2016
Decision
139d
Days
Class 2
Risk

K153226 is an FDA 510(k) clearance for the Solex 7 Intravascular Heat Exchange Catheter, ZOLL Start-Up Kit. This device is classified as a System, Hypothermia, Intravenous, Cooling (Class II - Special Controls, product code NCX).

Submitted by Zoll Circulation, Inc. (San Jose, US). The FDA issued a Cleared decision on March 24, 2016, 139 days after receiving the submission on November 6, 2015.

This device falls under the Neurology FDA review panel. Regulated under 21 CFR 870.5900.

Submission Details

510(k) Number K153226 FDA.gov
FDA Decision Cleared Substantially Equivalent - Abbreviated 510(k) (SESU)
Date Received November 06, 2015
Decision Date March 24, 2016
Days to Decision 139 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF

Device Classification

Product Code NCX - System, Hypothermia, Intravenous, Cooling
Device Class Class II - Special Controls
CFR Regulation 21 CFR 870.5900