meddevicedb.com FDA Device Reference

Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118

K251048 Class II Special
Decision Date
2025-05-02
Sponsor / Applicant
STERIS Corporation

Technical Specification

510(k) Submission ID K251048
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2025-05-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118 received FDA 510(k) clearance under submission number K251048, 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 2025-05-02.

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.