meddevicedb.com FDA Device Reference

ONE TRAY SEALED STERILIZATION CONTAINER

K052567 Class II Traditional
Decision Date
2006-03-13
Sponsor / Applicant
Sterile Containment Technology, LLC

Technical Specification

510(k) Submission ID K052567
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2006-03-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONE TRAY SEALED STERILIZATION CONTAINER received FDA 510(k) clearance under submission number K052567, sponsored by Sterile Containment Technology, LLC. 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 2006-03-13.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.