Source document or public record
FDA 510(k) K214122 — BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel
FDA 510(k) index record K214122. Device: BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel. Applicant as listed: Becton, Dickinson and Company. Decision date: 2022-07-28.
Source
"device_name": "BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K214122.
Device name: BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel. Applicant as listed: Becton, Dickinson and Company.
Decision date: 2022-07-28. Decision wording: Substantially Equivalent.
Product code: PCI. Regulation: 21 CFR 866.3990. Medical specialty: Microbiology.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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