Cleared Traditional

Servator C SALF Solution

K190063 · S.A.L.F. Spa · Gastroenterology & Urology
Aug 2019
Decision
211d
Days
Class 2
Risk

About This 510(k) Submission

K190063 is an FDA 510(k) clearance for the Servator C SALF Solution, a System And Accessories, Isolated Heart, Transport And Preservation (Class II — Special Controls, product code MSB), submitted by S.A.L.F. Spa (Cenate Sotto, IT). The FDA issued a Cleared decision on August 14, 2019, 211 days after receiving the submission on January 15, 2019. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5880.

Submission Details

510(k) Number K190063 FDA.gov
FDA Decision Cleared SESE
Date Received January 15, 2019
Decision Date August 14, 2019
Days to Decision 211 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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