meddevicedb.com FDA Device Reference

Steripack cases and Tray Systems

K193066 Class II Traditional
Decision Date
2020-08-06
Sponsor / Applicant
Avalign Technologies, Inc.

Technical Specification

510(k) Submission ID K193066
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2020-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Steripack cases and Tray Systems received FDA 510(k) clearance under submission number K193066, sponsored by Avalign Technologies, 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 2020-08-06.

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.