meddevicedb.com FDA Device Reference

Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not finalized) Sleeved IC 3 Plus (name not finalized) Sleeved IC 3 Plus Pocket (name not finalized) (N/A)

K251468 Class II Traditional
Decision Date
2025-10-03
Sponsor / Applicant
Hollister Incorporated

Technical Specification

510(k) Submission ID K251468
Product Code EZD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2025-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not finalized) Sleeved IC 3 Plus (name not finalized) Sleeved IC 3 Plus Pocket (name not finalized) (N/A) received FDA 510(k) clearance under submission number K251468, sponsored by Hollister Incorporated. 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 2025-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code EZD and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.