Source document or public record
FDA 510(k) K242367 — BIOFIRE FILMARRAY Gastrointestinal (GI) Panel
FDA 510(k) index record K242367. Device: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel. Applicant as listed: Biofire Diagnostics, LLC. Decision date: 2024-11-07.
Source
"device_name": "BIOFIRE FILMARRAY Gastrointestinal (GI) 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 K242367.
Device name: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel. Applicant as listed: Biofire Diagnostics, LLC.
Decision date: 2024-11-07. Decision wording: Substantially Equivalent.
Product code: PCH. 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.
Interested in these solutions?
Submit a sourcing request with the assays, volumes, and timeline of your own project.