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VERIFY Spore Test Strip for S40 Sterilant Concentrate

K231746 Class II Traditional
Decision Date
2023-09-11
Sponsor / Applicant
STERIS Corporation

Technical Specification

510(k) Submission ID K231746
Product Code OVY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6887
Decision Date 2023-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY Spore Test Strip for S40 Sterilant Concentrate received FDA 510(k) clearance under submission number K231746, 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 2023-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code OVY and 21 CFR 880.6887, within the General Hospital review panel as a Class II device.