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

CRP DIAGNOSTIC ASSAY

K Number: K050836 · Decision Aug 8, 2005
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
10
Review Days
129

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Basic Information

Device Name
CRP DIAGNOSTIC ASSAY
K Number
K050836
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. Srl
Date Received
April 1, 2005
Decision Date
August 8, 2005
Product Code
DCK
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
DCK C-Reactive Protein, Antigen, Antiserum, And Control

Similar 510(k) Clearances

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Other Clearances by Sentinel Ch. Srl

K Number Device Name
K070971 MODIFICATION TO SENTINEL CLIN CHEM CAL
K051447 SENTINEL PANCREATIC AMYLASE
K051114 SENTINEL AMMONIA ULTRA DIAGNOSTIC ASSAY
K051111 SENTINEL UIBC LIQUID
K051452 SENTINEL CLIN CHEM CAL
K051456 SENTINEL CERULOPLASMIN
K051115 SENTINEL IRON LIQUID
K051457 SENTINEL PLASMAPROTEINS CAL 3X
K051444 SENTINEL CHOLINESTERASE LIQUID