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

CINtec Histology

K Number: K212176 · Decision Dec 10, 2021
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
1
Applicant Total
48
Review Days
151

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Basic Information

Device Name
CINtec Histology
K Number
K212176
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.1865
Medical Specialty
Pathology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ventana Medical Systems, Inc.
Date Received
July 12, 2021
Decision Date
December 10, 2021
Product Code
PRB
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
PRB Cervical Intraepithelial Neoplasia (Cin) Test System

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