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VERIFY STEAM Integrating Indicator, VERIFY STEAM Integrating Indicator 5CM

K213412 Class II Traditional
Decision Date
2022-01-21
Sponsor / Applicant
Steris Corparation

Technical Specification

510(k) Submission ID K213412
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2022-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY STEAM Integrating Indicator, VERIFY STEAM Integrating Indicator 5CM received FDA 510(k) clearance under submission number K213412, sponsored by Steris Corparation. 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 2022-01-21.

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.