FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

CRP Vario

K Number: K192118 · Decision Nov 8, 2019
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
12
Review Days
94

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Basic Information

Device Name
CRP Vario
K Number
K192118
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SENTINEL CH. SpA
Date Received
August 6, 2019
Decision Date
November 8, 2019
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 SENTINEL CH. SpA

K Number Device Name
K242585 Cystatin C
K211058 Lp(a) Ultra
K193001 Albumin BCP
K173833 CRP Vario
K141728 ACE CALIBRATOR
K102706 CKMB UDR ASSAY
K083602 KAPPA LIGHT CHAINS
K083601 LAMBDA LIGHT CHAINS
K081533 SENTINEL PLASMAPROTEINS CAL 3X
K073634 MULTIGENT CREATININE (ENZYMATIC) ASSAY
Search all 12 clearances from SENTINEL CH. SpA →