Atlas FDA

cobas HCV

FDA 510(k) clearance K221007 · decided 2022-11-04

Clearance details

K-number
K221007
Device name
cobas HCV
Applicant
Roche Molecular Systems, Inc.
Decision
Substantially Equivalent
Date received
2022-04-05
Decision date
2022-11-04
Days to decision
213 days
Clearance type
Traditional
Product code
MZP
Device class
2
Regulation number
866.3170
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Pleasanton, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
cobas HCV (K252484)Roche Molecular Systems, Inc.2025-11-03
Alinity m HCV (K252102)Abbott Molecular, Inc.2025-09-25
Aptima HCV Quant Dx Assay (K233352)Hologic, Inc.2024-07-24

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