meddevicedb.com FDA Device Reference

3M™ Attest™ Super Rapid Vaporized Hydrogen Peroxide Clear Challenge Pack 1295PCD (1295PCD)

K241542 Class II Special
Decision Date
2024-06-27
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K241542
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2024-06-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M™ Attest™ Super Rapid Vaporized Hydrogen Peroxide Clear Challenge Pack 1295PCD (1295PCD) received FDA 510(k) clearance under submission number K241542, sponsored by 3M Company. 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 2024-06-27.

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.