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

CRP Vario

K Number: K173833 · Decision Sep 27, 2018
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
18
Applicant Total
12
Review Days
283

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Basic Information

Device Name
CRP Vario
K Number
K173833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SENTINEL CH. SpA
Date Received
December 18, 2017
Decision Date
September 27, 2018
Product Code
NQD
Advisory Committee
Immunology
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
NQD Cardiac C-Reactive Protein, Antigen, Antiserum, And Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NQD), 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
K192118 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 →