meddevicedb.com FDA Device Reference

PillCam SB 3 capsule endoscopy system, PillCam Software 9.0E

K211684 Class II Traditional
Decision Date
2021-08-27
Sponsor / Applicant
Given Imaging Ltd. (Medtronic)

Technical Specification

510(k) Submission ID K211684
Product Code NEZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1300
Decision Date 2021-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PillCam SB 3 capsule endoscopy system, PillCam Software 9.0E received FDA 510(k) clearance under submission number K211684, sponsored by Given Imaging Ltd. (Medtronic). The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2021-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code NEZ and 21 CFR 876.1300, within the Gastroenterology, Urology review panel as a Class II device.