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

IRON REAGENT

K Number: K964913 · Decision Feb 20, 1997
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
66
Applicant Total
18
Review Days
73

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Basic Information

Device Name
IRON REAGENT
K Number
K964913
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1410
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Derma Media Lab., Inc.
Date Received
December 9, 1996
Decision Date
February 20, 1997
Product Code
JIY
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
JIY Photometric Method, Iron (Non-Heme)

Similar 510(k) Clearances

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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
K964915 MAGNESIUM
K965134 ALT/SGPT
K964914 ALKALINE PHOSPHATASE
K965126 AST/SGOT
K964916 GAMMA-GLUTAMYL TRANSPEPTIDASE
Search all 18 clearances from Derma Media Lab., Inc. →