FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MAGNESIUM

K Number: K964915 · Decision Mar 26, 1997
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
18
Review Days
107

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Basic Information

Device Name
MAGNESIUM
K Number
K964915
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Derma Media Lab., Inc.
Date Received
December 9, 1996
Decision Date
March 26, 1997
Product Code
JGJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JGJ Photometric Method, Magnesium

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JGJ), ordered by most recent decision date.

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Other Clearances by Derma Media Lab., Inc.

K Number Device Name
K971309 UREA
K970664 GLUCOSE REAGENT
K971072 CHOLESTEROL REAGENT
K971005 TRIGLYCERIDES
K970867 URIC ACID REAGENT
K964913 IRON REAGENT
K965134 ALT/SGPT
K964914 ALKALINE PHOSPHATASE
K965126 AST/SGOT
K964916 GAMMA-GLUTAMYL TRANSPEPTIDASE
Search all 18 clearances from Derma Media Lab., Inc. →