meddevicedb.com FDA Device Reference

CALCIUM (ARSENAZO III) REAGENT

K894204 Class II Traditional
Decision Date
1989-10-04
Sponsor / Applicant
Sigma Diagnostics, Inc.

Technical Specification

510(k) Submission ID K894204
Product Code CJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1145
Decision Date 1989-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALCIUM (ARSENAZO III) REAGENT received FDA 510(k) clearance under submission number K894204, sponsored by Sigma Diagnostics, Inc.. 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 1989-10-04.

Classification & Regulation

This clearance is catalogued under FDA product code CJY and 21 CFR 862.1145, within the Clinical Chemistry review panel as a Class II device.