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| Trade Name | COBAS TAQMAN HBV TEST |
| Classification Name | hepatitis viral b dna detection |
| Generic Name | cobastaqman hbv test for use with the high pure system |
| Applicant | ROCHE MOLECULAR SYSTEMS, INC. |
| PMA Number | P050028 |
| Date Received | 08/02/2005 |
| Decision Date | 09/04/2008 |
| Product Code | |
| Docket Number | 08M-0501 |
| Notice Date | 09/11/2008 |
| Advisory Committee |
Microbiology |
| Expedited Review Granted? | No |
| Combination Product |
No
|
| Information About: |
Labeling, Approval Order, Summary of Safety and Effectiveness |
Approval Order Statement Approval for cobas taqman hbv test for use with the high pure system. This device is indicated for: the cobas taqman hbv test for use with the high pure system is an in vitro nucleic acid amplification test for the quantitation of hepatitis b virus (hbv) dna in human serum or plasma (edta), using the high pure viral nucleic acid kit for manual specimen preparation and the cobas taqman 48 analyzer for automated amplification and detection. The test is intended for use as an aid in the management of patients with chronic hbv infection undergoing anti-viral therapy. The assay can be used to measure hbv dna levels at baseline and during treatment to aid in assessing response to treatment. The results from the cobas taqman hbv test must be interpreted within the context of all relevant clinical and laboratory findings. Assay performance characteristics have been established for individuals treated with adefovir dipivoxil. Assay performance for determining the state of hbv infection has not been established. The cobas taqman hbv test is not intended for use as a screening test for blood or blood products for the presence of hbv or as a diagnostic test to confirm the presence of hbv infection. |
| Approval Order |
Approval Order
|
| Supplements: |
S001 S002 S003 S004 S005 S006 S007 S008 S011 S012 S013 S015 S016 S017 S019 S020 S021 S022 S023 S024 S025 S026 S027 S028 S029 S030 S031 S032 |