Cleared Special

K173955 - Mic-Key* SF Over-the-Wire Stoma Measuring Device
(FDA 510(k) Clearance)

Jan 2018
Decision
29d
Days
Class 2
Risk

K173955 is an FDA 510(k) clearance for the Mic-Key* SF Over-the-Wire Stoma Measuring Device. This device is classified as a Tubes, Gastrointestinal (and Accessories) (Class II - Special Controls, product code KNT).

Submitted by Halyard Health, Inc. (Alpharetta, US). The FDA issued a Cleared decision on January 26, 2018, 29 days after receiving the submission on December 28, 2017.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K173955 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received December 28, 2017
Decision Date January 26, 2018
Days to Decision 29 days
Submission Type Special
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code KNT — Tubes, Gastrointestinal (and Accessories)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5980

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