FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Yumizen C1200 CRP

K Number: K192028 · Decision Jun 25, 2020
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
17
Review Days
335

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Basic Information

Device Name
Yumizen C1200 CRP
K Number
K192028
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HORIBA ABX SAS
Date Received
July 26, 2019
Decision Date
June 25, 2020
Product Code
DCK
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DCK C-Reactive Protein, Antigen, Antiserum, And Control

Similar 510(k) Clearances

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

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Other Clearances by HORIBA ABX SAS

K Number Device Name
K232946 Yumizen H2500
K193649 Yumizen C1200 Creatinine PAP
K193525 Yumizen C1200 Immunoglobulin A, Yumizen C1200 Immunoglobulin G, Yumizen C1200 Immunoglobulin M
K191562 Yumizen C1200 Ferritin, Yumizen C1200 Transferrin, Yumizen C1200 Rheumatoid Factor
K191993 Yumizen C1200 CRP
K191245 Yumizen C1200 ALP, Yumizen C1200 Albumin
K191396 Yumizen C1200 Calcium AS, Yumizen C1200 Creatinine Jaffe
K170353 ABX MICROS ES 60 OT and ABX MICROS ES 60 CT
K151133 PENTRA XLR
K141161 ABX MICROS ES 60 CT; (OPEN TUBE MODEL), (CLOSE TUBE MODEL)
Search all 17 clearances from HORIBA ABX SAS →