meddevicedb.com FDA Device Reference

REAGENT FOR DETERM. CHLORIDE IN HUMAN/SM

K800683 Class II Traditional
Decision Date
1980-05-28
Sponsor / Applicant
Diagnostic Solutions, Inc.

Technical Specification

510(k) Submission ID K800683
Product Code CHJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1170
Decision Date 1980-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAGENT FOR DETERM. CHLORIDE IN HUMAN/SM received FDA 510(k) clearance under submission number K800683, sponsored by Diagnostic Solutions, 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 1980-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code CHJ and 21 CFR 862.1170, within the Clinical Chemistry review panel as a Class II device.