Atlas FDA

BD CTGCTV2

FDA 510(k) clearance K210585 · decided 2022-05-10

Clearance details

K-number
K210585
Device name
BD CTGCTV2
Applicant
Becton, Dickinson and Company
Decision
Substantially Equivalent
Date received
2021-02-26
Decision date
2022-05-10
Days to decision
438 days
Clearance type
Traditional
Product code
QEP
Device class
2
Regulation number
866.3393
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Sparks, MD, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989 recall (Z-0588-2025)Becton Dickinson & Co.2024-12-03

PMA approvals by this applicant

RecordFirmDate
BD ONCLARITY HPV ASSAY (P160037/S022)Becton, Dickinson and Company2025-08-25
BD Onclarity HPV Assay (P160037/S023)Becton, Dickinson and Company2025-07-02
Onclarity HPV Assay (P160037/S021)Becton, Dickinson and Company2025-03-12
BD Onclarity™ HPV Assay (P160037/S020)Becton, Dickinson and Company2024-11-05
BD Onclarity HPV Assay (P160037/S017)Becton, Dickinson and Company2024-05-14
BD Onclarity™ HPV Assay (P160037/S019)Becton, Dickinson and Company2024-04-18
BD Onclarity HPV Assay (P160037/S018)Becton, Dickinson and Company2023-11-20
BD Onclarity HPV (P160037/S016)Becton, Dickinson and Company2023-11-15