Atlas FDA

VENTANA MMR RxDx Panel (Solid Tumors with dMMR status)

FDA premarket approval P210001/S007 · decided 2022-11-10

Approval details

PMA number
P210001
Supplement
S007
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VENTANA MMR RxDx Panel (Solid Tumors with dMMR status)
Applicant
Ventana Medical Systems, Inc. (Roche Tissue Diagnostics)
Date received
2022-10-14
Decision date
2022-11-10
Days to decision
27 days
Decision code
OK30
Advisory committee
Pathology
Expedited review
No
Location
Tucson, AZ
Statement
Changes to a manufacturing process.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.