Cleared Traditional

FRESENIUS STERILE STAY SAFE CAP

K083542 · Fresenius Medical Care North America · Gastroenterology & Urology
Dec 2008
Decision
31d
Days
Class 2
Risk

About This 510(k) Submission

K083542 is an FDA 510(k) clearance for the FRESENIUS STERILE STAY SAFE CAP, a Set, Administration, For Peritoneal Dialysis, Disposable (Class II — Special Controls, product code KDJ), submitted by Fresenius Medical Care North America (Waltham,, US). The FDA issued a Cleared decision on December 29, 2008, 31 days after receiving the submission on November 28, 2008. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5630.

Submission Details

510(k) Number K083542 FDA.gov
FDA Decision Cleared SESE
Date Received November 28, 2008
Decision Date December 29, 2008
Days to Decision 31 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code KDJ — Set, Administration, For Peritoneal Dialysis, Disposable
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5630

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