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3M Attest Super Rapid Readout Steam Challenge Pack, 3M Attest Super Rapid 5 Steam-Plus Chaallenge Pack, 3M Attest Auto-reader, 3M Attest Auto-reader

K173519 Class II Traditional
Decision Date
2018-04-23
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K173519
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2018-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3M Attest Super Rapid Readout Steam Challenge Pack, 3M Attest Super Rapid 5 Steam-Plus Chaallenge Pack, 3M Attest Auto-reader, 3M Attest Auto-reader received FDA 510(k) clearance under submission number K173519, sponsored by 3M Company. 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 2018-04-23.

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.