FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

Urea Nitrogen2

K Number: K203771 · Decision May 31, 2022
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
8
Review Days
524

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Basic Information

Device Name
Urea Nitrogen2
K Number
K203771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Ireland Diagnostics Division
Date Received
December 23, 2020
Decision Date
May 31, 2022
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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K Number Device Name
K223317 Alkaline Phosphatase2
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K203530 Albumin BCP2
K203248 Albumin BCG2