meddevicedb.com FDA Device Reference

VERIFY STEAM Integrating Indicator

K152630 Class II Traditional
Decision Date
2016-05-12
Sponsor / Applicant
STERIS Corporation

Technical Specification

510(k) Submission ID K152630
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2016-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY STEAM Integrating Indicator received FDA 510(k) clearance under submission number K152630, sponsored by STERIS Corporation. 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 2016-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.