meddevicedb.com FDA Device Reference

TRIAGE TOTAL 3 CONTROLS AND CALIBRATION VERIFICATION SET

K093032 Class I Traditional
Decision Date
2009-11-13
Sponsor / Applicant
Biosite Incorporated

Technical Specification

510(k) Submission ID K093032
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2009-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIAGE TOTAL 3 CONTROLS AND CALIBRATION VERIFICATION SET received FDA 510(k) clearance under submission number K093032, sponsored by Biosite Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2009-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.