meddevicedb.com FDA Device Reference

RAICHEM(TM) SPIA(TM) MICROALBULMIN REAGENT

K903123 Class I Traditional
Decision Date
1990-09-14
Sponsor / Applicant
Reagents Applications, Inc.

Technical Specification

510(k) Submission ID K903123
Product Code JIQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1645
Decision Date 1990-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAICHEM(TM) SPIA(TM) MICROALBULMIN REAGENT received FDA 510(k) clearance under submission number K903123, sponsored by Reagents Applications, 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 1990-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code JIQ and 21 CFR 862.1645, within the Clinical Chemistry review panel as a Class I device.