meddevicedb.com FDA Device Reference

OTTO™ Disinfecting Cap

K252006 Class II Traditional
Decision Date
2026-03-27
Sponsor / Applicant
Icu Medical, Inc.

Technical Specification

510(k) Submission ID K252006
Product Code QBP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2026-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OTTO™ Disinfecting Cap received FDA 510(k) clearance under submission number K252006, sponsored by Icu Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2026-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code QBP and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.