Cleared Traditional

SHERPA PAK CARDIAC TRANSPORT SYSTEM

K133432 · Paragonix Technologies, Inc. · Gastroenterology & Urology
Feb 2014
Decision
108d
Days
Class 2
Risk

About This 510(k) Submission

K133432 is an FDA 510(k) clearance for the SHERPA PAK CARDIAC TRANSPORT SYSTEM, a System And Accessories, Isolated Heart, Transport And Preservation (Class II — Special Controls, product code MSB), submitted by Paragonix Technologies, Inc. (Providence, US). The FDA issued a Cleared decision on February 21, 2014, 108 days after receiving the submission on November 5, 2013. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5880.

Submission Details

510(k) Number K133432 FDA.gov
FDA Decision Cleared SESE
Date Received November 05, 2013
Decision Date February 21, 2014
Days to Decision 108 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code MSB — System And Accessories, Isolated Heart, Transport And Preservation
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5880

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