Ventana Medical Systems, Inc. - FDA 510(k) Cleared Devices
48
Total
46
Cleared
2
Denied
FDA 510(k) cleared devices by Ventana Medical Systems, Inc. Pathology ✕
18 devices
Cleared
Dec 17, 2024
Roche Digital Pathology Dx
Pathology
92d
Not Cleared
Dec 05, 2024
VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail (08507023001)
Pathology
190d
Cleared
Jun 14, 2024
Roche Digital Pathology Dx (VENTANA DP 200)
Pathology
270d
Cleared
Dec 10, 2021
CINtec Histology
Pathology
151d
Not Cleared
Mar 04, 2017
CINtec Histology (50 tests), CINtec Histology (250 tests)
Pathology
285d
Cleared
Jul 16, 2015
Virtuoso System for IHC PR (1E2) using iScan HT
Pathology
275d
Cleared
Mar 20, 2014
VIRTUOSO SYSTEM FOR IHC ER (SP1) WITH BENCHMARK ULTRA STAINER
Pathology
24d
Cleared
Nov 22, 2013
VIRTUOSO SYSTEM FOR IHC ER (SPI)
Pathology
268d
Cleared
Sep 26, 2013
VIRTUOSO SYSTEM FOR IHC HER2 (4B5)
Pathology
492d
Cleared
Sep 19, 2013
VIRTUOSO SYSTEM FOR IHC PR (1E2) BENCHMARK ULTRA STAINER
Pathology
427d
Cleared
Sep 06, 2013
VIRTUOSO SYSTEM FOR IHC KI-67 (30-9)
Pathology
519d
Cleared
Dec 17, 2012
CONFIRM ANTI-ESTROGEN RECEPTOR (SP1) RABBIT MONOCLONAL PRIMARY ANTIBODY
Pathology
719d