Atlas FDA

BD MAX(TM) ENTERIC BACTERIAL PANEL;BD MAX(TM) INSTRUMENT

FDA 510(k) clearance K140111 · decided 2014-05-06

Clearance details

K-number
K140111
Device name
BD MAX(TM) ENTERIC BACTERIAL PANEL;BD MAX(TM) INSTRUMENT
Applicant
Becton, Dickinson and Company
Decision
Substantially Equivalent
Date received
2014-01-15
Decision date
2014-05-06
Days to decision
111 days
Clearance type
Traditional
Product code
PCI
Device class
2
Regulation number
866.3990
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Sparks, MD, 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
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PanNAT STEC Test (K173330)Micronics, Inc.2018-06-01
Great Basin Stool Bacterial Pathogens Panel (K163571)Great Basin Scientific, Inc.2017-07-12

Recalls involving this device

No recalls on record reference this clearance.

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