PMA P100001S002
- Device
- VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBE REAGENT PACK AND CALIBRATOR
- Applicant
- Ortho-Clinical Diagnostics
- PMA number
- P100001
- Supplement
- S002
- Product code
- LOM
- Decision date
- 2012-10-17
- Classification
- Test, Hepatitis B (b Core, Be Antigen, Be Antibody, B Core Igm)
- Generic name
- Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
- Approval order statement
- CHANGE TO THE MANUFACTURING PROCESS AND STORAGE CONDITIONS OF THE ANTIFOAM SOLUTION.
Current openFDA PMA Record#
- Device
- VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HBE REAGENT PACK AND CALIBRATOR
- Applicant
- Ortho-Clinical Diagnostics
- PMA number
- P100001
- Supplement
- S002
- Product code
- LOM
- Generic name
- Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
- Decision date
- 2012-10-17
- Decision code
- OK30
- Date received
- 2012-09-19
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE TO THE MANUFACTURING PROCESS AND STORAGE CONDITIONS OF THE ANTIFOAM SOLUTION.