Cleared Traditional

CapsoCam Plus (SV-3) Capsule Endoscope System

K161773 · CapsoVision, Inc. · Gastroenterology & Urology
Oct 2016
Decision
115d
Days
Class 2
Risk

About This 510(k) Submission

K161773 is an FDA 510(k) clearance for the CapsoCam Plus (SV-3) Capsule Endoscope System, a System, Imaging, Gastrointestinal, Wireless, Capsule (Class II — Special Controls, product code NEZ), submitted by CapsoVision, Inc. (Saratoga, US). The FDA issued a Cleared decision on October 21, 2016, 115 days after receiving the submission on June 28, 2016. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1300.

Submission Details

510(k) Number K161773 FDA.gov
FDA Decision Cleared SESE
Date Received June 28, 2016
Decision Date October 21, 2016
Days to Decision 115 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code NEZ — System, Imaging, Gastrointestinal, Wireless, Capsule
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1300

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