meddevicedb.com FDA Device Reference

Instant 20s Indicator

K210481 Class II Traditional
Decision Date
2021-12-14
Sponsor / Applicant
True Indicating, LLC

Technical Specification

510(k) Submission ID K210481
Product Code MTC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2021-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Instant 20s Indicator received FDA 510(k) clearance under submission number K210481, sponsored by True Indicating, LLC. 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 2021-12-14.

Classification & Regulation

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