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

PHOSPHORUS (INORGANIC) TEST SYSTEM

K Number: K910296 · Decision Feb 27, 1991
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
20
Review Days
35

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Basic Information

Device Name
PHOSPHORUS (INORGANIC) TEST SYSTEM
K Number
K910296
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biochemical Trade, Inc.
Date Received
January 23, 1991
Decision Date
February 27, 1991
Product Code
CEO
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

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K Number Device Name
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K905790 TOTAL PROTEIN REAGENT SET
K905619 CREATININE (RATE) REAGENT SET
K905650 KINETIC ALKALINE PHOSPHATASE DETERMINATION
K905651 KINETIC AMYLASE DETERMINATION
K905649 GAMMA-GLUTAMYL TRANSFERASE DETERMINATION
K905588 CREATINE KINASE UV REAGENT SET
K871547 ULTRA-VIOLET BUN REAGENT KIT (RATE)
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