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VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR FOR VAPORIZED (VH2O2) STERILIZATION PROCESSES

K090514 Class II Special
Decision Date
2009-03-16
Sponsor / Applicant
STERIS Corporation

Technical Specification

510(k) Submission ID K090514
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2009-03-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR FOR VAPORIZED (VH2O2) STERILIZATION PROCESSES received FDA 510(k) clearance under submission number K090514, sponsored by STERIS Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2009-03-16.

Classification & Regulation

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