Cleared Traditional

Percutaneous Entry Set, Skinny Needle(R) with Chiba Tip, Disposable Two-part Trocar Needle

K183035 · Cook Incorporated · Gastroenterology & Urology
May 2019
Decision
197d
Days
Risk

About This 510(k) Submission

K183035 is an FDA 510(k) clearance for the Percutaneous Entry Set, Skinny Needle(R) with Chiba Tip, Disposable Two-part Trocar Needle, a Catheter, Nephrostomy, submitted by Cook Incorporated (Bloomington, US). The FDA issued a Cleared decision on May 17, 2019, 197 days after receiving the submission on November 1, 2018. This device falls under the Gastroenterology & Urology review panel.

Submission Details

510(k) Number K183035 FDA.gov
FDA Decision Cleared SESK
Date Received November 01, 2018
Decision Date May 17, 2019
Days to Decision 197 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code LJE — Catheter, Nephrostomy
Device Class

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