meddevicedb.com FDA Device Reference

VERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein (CPP) Indicator

DEN230085 Class II Direct
Decision Date
2024-11-12
Sponsor / Applicant
Steris

Technical Specification

510(k) Submission ID DEN230085
Product Code SDC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6930
Decision Date 2024-11-12
Clearance Pathway Direct

Official Documentation

No FDA summary/statement PDF is linked for this clearance in the current dataset. Consult the product code and regulation citation above to locate predicate documentation.

Clearance Summary

VERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein (CPP) Indicator received FDA 510(k) clearance under submission number DEN230085, sponsored by Steris. The device was reviewed via the Direct premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code SDC and 21 CFR 880.6930, within the General Hospital review panel as a Class II device.