PMA P100020
- Device
- cobas® HPV
- Applicant
- Roche Molecular Systems, Inc.
- PMA number
- P100020
- Supplement
- S054
- Product code
- MAQ
- Decision date
- 2026-10-27
- Generic name
- KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
- Approval order statement
- to change the manufacturing process for oligonucleotides
Current openFDA PMA Record#
- Device
- cobas® HPV
- Applicant
- Roche Molecular Systems, Inc.
- PMA number
- P100020
- Supplement
- S066
- Product code
- MAQ
- Generic name
- KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
- Decision date
- 2026-10-27
- Decision code
- OK30
- Date received
- 2026-09-30
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- to change the manufacturing process for oligonucleotides