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

MEGNESIUM REAGENT KIT

K Number: K821102 · Decision May 5, 1982
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
26
Review Days
15

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Basic Information

Device Name
MEGNESIUM REAGENT KIT
K Number
K821102
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Anco Medical Reagents & Assoc.
Date Received
April 20, 1982
Decision Date
May 5, 1982
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

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Other Clearances by Anco Medical Reagents & Assoc.

K Number Device Name
K842440 SICKLE CELL STAT A/S HETEROZYGOUS-ERYTH
K831871 SICKLE-HEME A/S CONTROLS & A/A CONTROL
K821658 HEMOGLOBIN REAGENT
K821526 ACID PHOSPHATASE REAGENT SET
K820951 ENZYMATIC CHOLESTEROL KIT
K820491 SGPT REAGENT SET
K820500 TOTAL LIPID REAGENT SET
K820466 SGOT REAGENT SET
K812837 ALKALINE PHOSPHATASE REAGENT SET
K813415 UREA NITROGEN REAGENT SET
Search all 26 clearances from Anco Medical Reagents & Assoc. →