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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.
 
Devicecobas® EZH2 Mutation Test
Generic NameSomatic gene mutation detection system
ApplicantRoche Molecular System, Inc.
4300 Hacienda Dr.
Pleasanton, CA 94588
PMA NumberP200014
Supplement NumberS009
Date Received09/11/2024
Decision Date10/10/2024
Withdrawal Date07/06/2026
Product Code OWD 
Advisory Committee Pathology
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  
manufacturing process change
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