COBAS AMPLIPREP/COBAS TAQMAN HCV TEST
FDA premarket approval P060030 · decided 2008-10-30
Approval details
- PMA number
- P060030
- Trade name
- COBAS AMPLIPREP/COBAS TAQMAN HCV TEST
- Generic name
- Assay, hybridization and/or nucleic acid amplification for detection of hepatitis c rna,hepatitis c virus
- Applicant
- Roche Molecular Systems, Inc.
- Date received
- 2006-10-27
- Decision date
- 2008-10-30
- Days to decision
- 734 days
- Decision code
- APRL
- Product code
- MZP
- Advisory committee
- Microbiology
- Expedited review
- No
- Location
- Pleasanton, CA
- Statement
- APPROVAL FOR THE COBASAMPLIPREP/COBAS TAQMAN HCV TEST. THIS DEVICE IS AN IN VITRO NUCLEIC ACID AMPLIFICATION LESTFOR THE QUANTITATION OF HEPATITIS C VIRAL (HCV) RNA IN HUMAN PLASMA OR SERUM OF HCV-INFECTEDINDIVIDUALS USING THE COBAS AMPLIPREP INSTRUMENT FOR AUTOMATED SPECIMEN PROCESSING AND THECOBAS TAQMAN ANALYZER OR THE COBAS TAQMAN 48 ANALYZER FOR AUTOMATED AMPLIFICATION ANDDETECTION. SPECIMENS CONTAINING HCV GENOTYPES 1 - 6 HAVE BEEN VALIDATED FOR QUANTITATION INTHE ASSAY. THE COBAS AMPLIPRE
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| cobas® BV/CV (K260021) | Roche Molecular Systems, Inc. | 2026-07-16 |
| cobas CT/NG for use on the cobas 5800/6800/8800 systems; cobas TV/MG for use on the cobas 5800/6800/8800 systems (K260917) | Roche Molecular Systems, Inc. | 2026-07-08 |
| cobas liat CT/NG/MG nucleic acid test (K253759) | Roche Molecular Systems, Inc. | 2026-05-15 |
| cobas liat CT/NG nucleic acid test (K253756) | Roche Molecular Systems, Inc. | 2026-05-15 |
| cobas liat Bordetella panel nucleic acid test (K243753) | Roche Molecular Systems, Inc. | 2025-11-20 |
| cobas CMV (K252481) | Roche Molecular Systems, Inc. | 2025-11-03 |
| cobas HCV (K252484) | Roche Molecular Systems, Inc. | 2025-11-03 |
| cobas Respiratory 4-flex for use on the cobas 5800/6800/8800 Systems (K243455) | Roche Molecular Systems, Inc. | 2025-07-31 |