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EMDS(TM) MAGNESIUM TESTPACKS, #67671/95

K863002 Class I Traditional
Decision Date
1986-08-19
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K863002
Product Code JGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1495
Decision Date 1986-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMDS(TM) MAGNESIUM TESTPACKS, #67671/95 received FDA 510(k) clearance under submission number K863002, 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 1986-08-19.

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.