Cobas 4800 BRAF V600 Mutation Test
FDA premarket approval P110020/S023 · decided 2017-11-13
Approval details
- PMA number
- P110020
- Supplement
- S023
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Cobas 4800 BRAF V600 Mutation Test
- Generic name
- Somatic gene mutation detection system
- Applicant
- Roche Molecular Systems, Inc.
- Date received
- 2017-10-30
- Decision date
- 2017-11-13
- Days to decision
- 14 days
- Decision code
- OK30
- Product code
- OWD
- Advisory committee
- Pathology
- Expedited review
- No
- Location
- Pleasanton, CA
- Statement
- Scale-up production of a bulk reagent.
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510(k) clearances by this applicant
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|---|---|---|
| cobas® BV/CV (K260021) | Roche Molecular Systems, Inc. | 2026-07-16 |
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| cobas HCV (K252484) | Roche Molecular Systems, Inc. | 2025-11-03 |
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