meddevicedb.com FDA Device Reference

MAGNESIUM TEST ITEM NUMBER: 65419

K894508 Class I Traditional
Decision Date
1989-08-31
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K894508
Product Code JGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1495
Decision Date 1989-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAGNESIUM TEST ITEM NUMBER: 65419 received FDA 510(k) clearance under submission number K894508, sponsored by Em Diagnostic Systems, 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 1989-08-31.

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.