FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

N Latex Cystatin C; N Protein Standard UY

K Number: K171072 · Decision May 12, 2017
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
21
Applicant Total
19
Review Days
32

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Basic Information

Device Name
N Latex Cystatin C; N Protein Standard UY
K Number
K171072
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1225
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Healthcare Diagnostics Products GmbH
Date Received
April 10, 2017
Decision Date
May 12, 2017
Product Code
NDY
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
NDY Test, Cystatin C

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K233663 N Antisera to Human Immunoglobulins (IgG, IgA, and IgM)
K220728 vWF Ag
K212559 CardioPhase® hsCRP
DEN200067 INNOVANCE VWF Ac
K212379 N Latex FLC kappa, N Latex FLC lambda
K201496 N Latex FLC kappa, N Latex FLC lambda
K193047 N Latex FLC kappa, N Latex FLC lambda
K190879 N Latex FLC kappa, N Latex FLC lambda
K182098 N Latex FLC kappa assay, N Latex FLC lambda assay
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