FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇷 Greece

Medicon Hellas Albumin, Medicon Hellas Calcium, Medicon Hellas Creatinine, Medicon Hellas Urea Nitrogen, Medicon Hellas Glucose, Medicon Hellas Total Bilirubin, Medicon Hellas Direct Bilirubin

K Number: K200898 · Decision Sep 21, 2021
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
119
Applicant Total
3
Review Days
536

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Basic Information

Device Name
Medicon Hellas Albumin, Medicon Hellas Calcium, Medicon Hellas Creatinine, Medicon Hellas Urea Nitrogen, Medicon Hellas Glucose, Medicon Hellas Total Bilirubin, Medicon Hellas Direct Bilirubin
K Number
K200898
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1035
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicon Hellas S.A
Date Received
April 3, 2020
Decision Date
September 21, 2021
Product Code
CIX
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
CIX Bromcresol Green Dye-Binding, Albumin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CIX), ordered by most recent decision date.

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Other Clearances by Medicon Hellas S.A

K Number Device Name
K232404 CHOLESTEROL; HDL-cholesterol ; LDL-cholesterol; TRIGLYCERIDES
K062746 FERRITIN-LATEX, MODELS 1418-2070, 1418-0279