PMA P170025S012
- Device
- Aptima HBV Quant Assay
- Applicant
- Hologic, Inc.
- PMA number
- P170025
- Supplement
- S012
- Product code
- MKT
- Decision date
- 2019-05-21
- Classification
- Hepatitis Viral B Dna Detection
- Generic name
- Hepatitis Viral B DNA Detection
- Approval order statement
- Remove QC release testing for a device ancillary kit.
Current openFDA PMA Record#
- Device
- Aptima HBV Quant Assay
- Applicant
- Hologic, Inc.
- PMA number
- P170025
- Supplement
- S012
- Product code
- MKT
- Generic name
- Hepatitis Viral B DNA Detection
- Decision date
- 2019-05-21
- Decision code
- OK30
- Date received
- 2019-04-19
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Remove QC release testing for a device ancillary kit.