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

AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS

K Number: K802159 · Decision Oct 10, 1980
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
16
Review Days
32

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Basic Information

Device Name
AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS
K Number
K802159
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Panmed, Inc.
Date Received
September 8, 1980
Decision Date
October 10, 1980
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

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K Number Device Name
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K802158 POSTASSIUM BUFFER SOL. & WASH SOLUTION
K802162 CO2 COLOR REAGENT & CO2 SAMPLE DILUENT
K802156 REAGENTS SERUM CREATINE USING TECHICON
K802163 CHLORIDE COLOR & CHLORIDE SAMPLE DILUENT
K802157 BCG REAGENT SERUM ALBUMIN W/TECHNICON
K802160 BUN COLOR REAGENT & BUN ACID USED
K802164 8-HYDROXYQUINOLINE, CRESOLPHTHALEIN COM.
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