PMA P080014S004
- Device
- CERVISTA HPV HR
- Applicant
- Hologic, Inc.
- PMA number
- P080014
- Supplement
- S004
- Product code
- MAQ
- Decision date
- 2010-10-26
- Classification
- Kit, Dna Detection, Human Papillomavirus
- Generic name
- KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
- Approval order statement
- CHANGES IN THE FILL VOLUME OF THE WASH BUFFER AND AN INCREASE IN SAMPLE SIZE OF THE INCOMING COMPONENTS BEING TESTED.
Current openFDA PMA Record#
- Device
- CERVISTA HPV HR
- Applicant
- Hologic, Inc.
- PMA number
- P080014
- Supplement
- S004
- Product code
- MAQ
- Generic name
- KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
- Decision date
- 2010-10-26
- Decision code
- OK30
- Date received
- 2010-10-05
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGES IN THE FILL VOLUME OF THE WASH BUFFER AND AN INCREASE IN SAMPLE SIZE OF THE INCOMING COMPONENTS BEING TESTED.