meddevicedb.com FDA Device Reference

RAICHEM(TM) MAGNESIUM REAGENT

K874822 Class I Traditional
Decision Date
1988-01-21
Sponsor / Applicant
Reagents Applications, Inc.

Technical Specification

510(k) Submission ID K874822
Product Code JGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1495
Decision Date 1988-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAICHEM(TM) MAGNESIUM REAGENT received FDA 510(k) clearance under submission number K874822, 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 1988-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code JGJ and 21 CFR 862.1495, within the Clinical Chemistry review panel as a Class I device.