Atlas FDA

cobas BKV

FDA 510(k) clearance K203220 · decided 2021-01-29

Clearance details

K-number
K203220
Device name
cobas BKV
Applicant
Roche Molecular Systems, Inc.
Decision
Substantially Equivalent
Date received
2020-11-02
Decision date
2021-01-29
Days to decision
88 days
Clearance type
Traditional
Product code
QLX
Device class
2
Regulation number
866.3183
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
Alinity m EBV (09N43-095) (K243489)Abbott Molecular, Inc.2025-07-28
Alinity m EBV AMP Kit (List No. 09N43-095), Alinity m EBV CTRL Kit (List No. 09N43-085), Alinity m EBV CAL Kit (List No. 09N43-075) (K212778)Abbott Molecular, Inc.2022-07-15
cobas EBV, cobas EBV/BKV Control Kit, cobas Buffer Negative Control Kit (DEN200015)Roche Molecular Systems, Inc.2020-07-30

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