Skip to content

Emds Magnesium (Mg) Test

by Em Diagnostic Systems, Inc. 510(k)

Active United States

510(k) K935183

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK935183 Date9 Dec 1993ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
JGJ
Device Class
Class I
Regulation
21 CFR Part 862.1495
Advisory Committee
Clinical Chemistry
FDA Decision
SESE Substantially Equivalent

Other devices from Em Diagnostic Systems, Inc.

See all devices from Em Diagnostic Systems, Inc. →