FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BUN

K Number: K781782 · Decision Jan 10, 1979
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
116
Applicant Total
50
Review Days
83

Basic Information

Device Name
BUN
K Number
K781782
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
GILFORD DIAGNOSTICS
Date Received
October 19, 1978
Decision Date
January 10, 1979
Product Code
CDQ
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
CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

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Other Clearances by GILFORD DIAGNOSTICS

K Number Device Name
K832094 BILIRUBIN CALIBRATORS & CONTROL
K831843 GILCHEM TOTAL BILIRUBIN REAGENT
K831844 DIRECT BILIRUBIN REAGENT
K823709 TRIGLYCERIDE REAGENT (UV)
K822739 AHBD
K822334 BILIRUBIN CALIBRATORS
K822289 CO2/CI STANDARDS
K822149 GILCHEM Y-GT REAGENT
K821719 AMMONIA REAGENT
K820975 GILCHEM ACID PHOSPHATASE REAGENT
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