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INFORM HER2 Dual ISH DNA Probe Cocktail assays

FDA premarket approval P100027/S030 · decided 2019-05-03

Approval details

PMA number
P100027
Supplement
S030
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
INFORM HER2 Dual ISH DNA Probe Cocktail assays
Generic name
Chromogenic in situ hybridization, nucleic acid amplification, HER2/NEU gene, breast cancer
Applicant
Ventana Medical Systems, Inc.
Date received
2019-02-13
Decision date
2019-05-03
Days to decision
79 days
Decision code
APPR
Product code
NYQ
Advisory committee
Pathology
Expedited review
No
Location
Tucson, AZ
Statement
Approval for the Ventana Medical Systems, Inc’s (Ventana) INFORM HER2 Dual ISH DNA Probe Cocktail is intended to determine HER2 gene status by enumeration of the ratio of the HER2 gene to Chromosome 17. The HER2 and Chromosome 17 probes are detected by light microscopy using two color chromogenic in situ hybridization (ISH) in formalin-fixed, paraffin-embedded human breast cancer tissue specimens following staining on a BenchMark XT or BenchMark ULTRA instrument. The INFORM HER2 Dual ISH DNA Pro

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