Cleared Traditional

K191715 - Endoscope Tip Protector - Sterile, Endoscope Tip Protector - Non-sterile
(FDA 510(k) Clearance)

Jan 2020
Decision
215d
Days
Class 2
Risk

K191715 is an FDA 510(k) clearance for the Endoscope Tip Protector - Sterile, Endoscope Tip Protector - Non-sterile. This device is classified as a Endoscopic Storage Cover (Class II - Special Controls, product code OCU).

Submitted by STERIS Corporation (Mentor, US). The FDA issued a Cleared decision on January 27, 2020, 215 days after receiving the submission on June 26, 2019.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Protect Delicate Parts Of The Endoscope During Transport And Storage. May Also Be Used To Protect During Sterilization..

Submission Details

510(k) Number K191715 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 26, 2019
Decision Date January 27, 2020
Days to Decision 215 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code OCU — Endoscopic Storage Cover
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Protect Delicate Parts Of The Endoscope During Transport And Storage. May Also Be Used To Protect During Sterilization.