Premarket Approval (PMA)

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.

• Device: cobas EGFR Mutation Test and cobas EGFR Mutation Test v2
• Generic Name: Somatic gene mutation detection system
• Applicant: Roche; 4300 Hacienda Dr.; P.O. Box 9002; Peasanton, CA 94588
• PMA Number: P120019
• Supplement Number: S030
• Date Received: 09/20/2019
• Decision Date: 10/10/2019
• Product Code: OWD
• Advisory Committee: Pathology
• Supplement Type: 30-Day Notice
• Supplement Reason: Process Change - Manufacturer/Sterilizer/Packager/Supplier
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No

Approval Order Statement  
Implement an alternate spectrophotometer for in-process QC testing.