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VERIFY 275 DEGREE F. 3-10 INDICATOR; 10 INDICATOR; 3 INDICATOR

K071895 Class II Abbreviated
Decision Date
2007-11-14
Sponsor / Applicant
STERIS Corporation

Technical Specification

510(k) Submission ID K071895
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2007-11-14
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIFY 275 DEGREE F. 3-10 INDICATOR; 10 INDICATOR; 3 INDICATOR received FDA 510(k) clearance under submission number K071895, sponsored by STERIS Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2007-11-14.

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.