meddevicedb.com FDA Device Reference

Terragene® Chemdye® Multivariable Chemical Indicator (CD40), Terragene® Chemdye® Chemical Process Indicator (CD42), Terragene® Cintape® Chemical Process Indicator Tape (CT40)

K232103 Class II Traditional
Decision Date
2024-04-05
Sponsor / Applicant
Terragene S.A.

Technical Specification

510(k) Submission ID K232103
Product Code QKM
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2024-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Terragene® Chemdye® Multivariable Chemical Indicator (CD40), Terragene® Chemdye® Chemical Process Indicator (CD42), Terragene® Cintape® Chemical Process Indicator Tape (CT40) received FDA 510(k) clearance under submission number K232103, sponsored by Terragene S.A.. 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 2024-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code QKM and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.