meddevicedb.com FDA Device Reference

Curos Jet Disinfecting Cap

K200299 Class II Traditional
Decision Date
2020-10-29
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K200299
Product Code QBP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2020-10-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Curos Jet Disinfecting Cap received FDA 510(k) clearance under submission number K200299, sponsored by 3M Company. 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 2020-10-29.

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.