Cleared Traditional

CapsoCam Plus (SV-3) Capsule Endoscopy System

K242643 · CapsoVision, Inc. · Gastroenterology & Urology
Dec 2024
Decision
92d
Days
Class 2
Risk

About This 510(k) Submission

K242643 is an FDA 510(k) clearance for the CapsoCam Plus (SV-3) Capsule Endoscopy 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 December 4, 2024, 92 days after receiving the submission on September 3, 2024. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1300.

Submission Details

510(k) Number K242643 FDA.gov
FDA Decision Cleared SESE
Date Received September 03, 2024
Decision Date December 04, 2024
Days to Decision 92 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

Similar Devices — NEZ System, Imaging, Gastrointestinal, Wireless, Capsule

All 45
CE Deliver (DLV)
K252480 · CapsoVision, Inc. · Dec 2025
PillCam? Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software
K240276 · Given Imaging Ltd. (D.B.A. Medtronic) · May 2024
NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether
K233229 · Anx Robotica Corporation · Jan 2024
PillCam SB 3 capsule endoscopy system, PillCam Software 9.0E
K230991 · Given Imaging Ltd. (Medtronic) · Jun 2023
NaviCam Small Bowel Capsule Endoscopy System
K221590 · Ankon Technologies Co., Ltd. · Dec 2022
PillCam SB 3 capsule endoscopy system, PillCam Software 9.0E
K211684 · Given Imaging Ltd. (Medtronic) · Aug 2021