KING DIAGNOSTICS MAGNESIUM REAGENT

Photometric Method, Magnesium

KING DIAGNOSTICS, INC.

The following data is part of a premarket notification filed by King Diagnostics, Inc. with the FDA for King Diagnostics Magnesium Reagent.

Pre-market Notification Details

Device IDK923927
510k NumberK923927
Device Name:KING DIAGNOSTICS MAGNESIUM REAGENT
ClassificationPhotometric Method, Magnesium
Applicant KING DIAGNOSTICS, INC. 6856 HAWTHORN PARK DR. Indianapolis,  IN  46220
ContactFrances Loh
CorrespondentFrances Loh
KING DIAGNOSTICS, INC. 6856 HAWTHORN PARK DR. Indianapolis,  IN  46220
Product CodeJGJ  
CFR Regulation Number862.1495 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-08-05
Decision Date1992-09-30

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