510(k) K912825

MAGNESIUM ASSAY KIT, CAT.# 100-12 by Diagnostic Chemicals, Ltd. (Usa) — Product Code JGJ

K912825 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals, Ltd. (Usa) for the device "MAGNESIUM ASSAY KIT, CAT.# 100-12". The FDA issued a decision of Substantially Equivalent on July 26, 1991. The device falls under product code JGJ (Photometric Method, Magnesium), a Class I device regulated under 21 CFR 862.1495. Diagnostic Chemicals, Ltd. (Usa) has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 26, 1991
Date Received
June 26, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Photometric Method, Magnesium
Device Class
Class I
Regulation Number
862.1495
Review Panel
CH
Submission Type