Atlas FDA

cobas® BV/CV

FDA 510(k) clearance K260021 · decided 2026-07-16

Clearance details

K-number
K260021
Device name
cobas® BV/CV
Applicant
Roche Molecular Systems, Inc.
Decision
Substantially Equivalent
Date received
2026-01-05
Decision date
2026-07-16
Days to decision
192 days
Clearance type
Traditional
Product code
PQA
Device class
2
Regulation number
866.3975
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Pleasanton, CA, US
Third-party review
No
Expedited review
No

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BD MAX Vaginal Panel, BD MAX System, BD Molecular Swab Collection Kit (K201017)Geneohm Sciences Canada, Inc. (Bd Life Sciences)2021-10-18
BD MAX Vaginal Panel (K191957)Geneohm Sciences Canada, Inc. (Bd Diagnostics)2019-10-21
Aptima BV Assay (K190452)Hologic, Inc.2019-05-23
Aptima CV/TV Assay (K190472)Hologic, Inc.2019-05-16
BD MAX Vaginal Panel, BD MAX Instrument (DEN160001)Geneohm Sciences Canada, Inc. (Bd Diagnostics)2016-10-28

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
cobas® HPV (P190028/S022)Roche Molecular Systems, Inc.2025-12-31
cobsa® BRAF V600 Mutation Test (P110020/S043)Roche Molecular Systems, Inc.2025-12-31
cobas® KRAS Mutation Test (P140023/S031)Roche Molecular Systems, Inc.2025-12-31
cobas® HPV (P100020/S064)Roche Molecular Systems, Inc.2025-12-31
COBAS HPV TEST (P100020/S063)Roche Molecular Systems, Inc.2025-12-15
cobas® HBV (P150014/S056)Roche Molecular Systems, Inc.2025-10-17
cobas HPV (P190028/S021)Roche Molecular Systems, Inc.2025-09-19
cobas HBV (P150014/S058)Roche Molecular Systems, Inc.2025-09-19