Atlas FDA

CINtec PLUS Cytology

FDA premarket approval P190024/S003 · decided 2021-05-20

Approval details

PMA number
P190024
Supplement
S003
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CINtec PLUS Cytology
Generic name
Immunocytochemistry assay, p16/Ki-67
Applicant
Ventana Medical Systems, Inc.
Date received
2021-02-22
Decision date
2021-05-20
Days to decision
87 days
Decision code
APPR
Product code
QKF
Advisory committee
Pathology
Expedited review
No
Location
Tucson, AZ
Statement
Approval for the dispenser resin replacement used in the injection molding process for six (6) dispenser parts.

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510(k) clearances by this applicant

RecordFirmDate
Roche Digital Pathology Dx (K242783)Ventana Medical Systems, Inc.2024-12-17
VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail (08507023001) (DEN240025)Ventana Medical Systems, Inc.2024-12-05
Roche Digital Pathology Dx (VENTANA DP 200) (K232879)Ventana Medical Systems, Inc.2024-06-14
CINtec Histology (K212176)Ventana Medical Systems, Inc.2021-12-10
VENTANA CD30 (Ber-H2) RxDx Assay (K172471)Ventana Medical Systems, Inc.2018-05-08
CINtec Histology (50 tests), CINtec Histology (250 tests) (DEN160019)Ventana Medical Systems, Inc.2017-03-04
Virtuoso System for IHC PR (1E2) using iScan HT (K142965)Ventana Medical Systems, Inc.2015-07-16
VIRTUOSO SYSTEM FOR IHC ER (SP1) WITH BENCHMARK ULTRA STAINER (K140465)Ventana Medical Systems, Inc.2014-03-20