Cleared Traditional

K173687 - Strange Bile Duct Stone Exploration Set (FDA 510(k) Clearance)

Dec 2017
Decision
14d
Days
Class 2
Risk

K173687 is an FDA 510(k) clearance for the Strange Bile Duct Stone Exploration Set. This device is classified as a Dislodger, Stone, Biliary (Class II - Special Controls, product code LQR).

Submitted by Cook Incorporated (Bloomington, US). The FDA issued a Cleared decision on December 15, 2017, 14 days after receiving the submission on December 1, 2017.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5010.

Submission Details

510(k) Number K173687 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received December 01, 2017
Decision Date December 15, 2017
Days to Decision 14 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code LQR — Dislodger, Stone, Biliary
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5010