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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceVENTANA FOLR1 (FOLR1-2.1) RxDx Assay
Generic NameImmunohistochemistry Assay, Antibody, FOLR1
Regulation Number864.1860
ApplicantVentana Medical Systems, Inc.
1910 E. Innovation Park Dr.
Tucson, AZ 85755
PMA NumberP220006
Supplement NumberS002
Date Received08/01/2023
Decision Date08/29/2023
Product Code QUL 
Advisory Committee Molecular Genetics
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Addition of two contract manufacturers as approved suppliers of parts/components.
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