Atlas FDA

VENTANA CLDN18 (43-14A) RxDx Assay

FDA premarket approval P230018/S001 · decided 2025-06-20

Approval details

PMA number
P230018
Supplement
S001
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VENTANA CLDN18 (43-14A) RxDx Assay
Generic name
Immunohistochemistry assay, antibody, claudin 18
Applicant
Ventana Medical Systems, Inc.
Date received
2025-05-21
Decision date
2025-06-20
Days to decision
30 days
Decision code
OK30
Product code
QZJ
Advisory committee
Pathology
Expedited review
No
Location
Tucson, AZ
Statement
qualification of an alternate supplier for assay kit component

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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