FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VENTANA CD30 (Ber-H2) RxDx Assay

K Number: K172471 · Decision May 8, 2018
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
52
Applicant Total
48
Review Days
266

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Basic Information

Device Name
VENTANA CD30 (Ber-H2) RxDx Assay
K Number
K172471
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5550
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ventana Medical Systems, Inc.
Date Received
August 15, 2017
Decision Date
May 8, 2018
Product Code
DEH
Advisory Committee
Immunology
Review Advisory Committee
MG
Third Party
N

Classifications

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

Product Code Device Name
DEH Lambda, Antigen, Antiserum, Control

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K121516 VIRTUOSO SYSTEM FOR IHC HER2 (4B5)
K122143 VIRTUOSO SYSTEM FOR IHC PR (1E2) BENCHMARK ULTRA STAINER
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