Documento fuente o registro público
FDA 510(k) K242492 — Multichem ID-G (09339892190); Multichem ID-G (SR102G); Multichem ID-G (SR102MG); Multichem ID-GNeg (09339906190); Multichem ID-GNeg (SR102N); Multichem ID-GNeg (SR102MN)
FDA 510(k) index record K242492. Device: Multichem ID-G (09339892190); Multichem ID-G (SR102G); Multichem ID-G (SR102MG); Multichem ID-GNeg (09339906190); Multichem ID-GNeg (SR102N); Multichem ID-GNeg (SR102MN). Applicant as listed: Techno-Path Manufacturing , Ltd.. Decision date: 2025-12-30.
Fuente
"device_name": "Multichem ID-G (09339892190); Multichem ID-G (SR102G); Multichem ID-G (SR102MG); Multichem ID-GNeg (09339906190); Multichem ID-GNeg (SR102N); Multichem ID-GNeg (SR102MN)"
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Review and references
Automated FDA record verification
2026-10-20
2026-10-23
professional use
FDA 510(k) public index record K242492.
Device name: Multichem ID-G (09339892190); Multichem ID-G (SR102G); Multichem ID-G (SR102MG); Multichem ID-GNeg (09339906190); Multichem ID-GNeg (SR102N); Multichem ID-GNeg (SR102MN). Applicant as listed: Techno-Path Manufacturing , Ltd..
Decision date: 2025-12-30. Decision wording: Substantially Equivalent.
Product code: QCH. Regulation: 21 CFR 866.3920. 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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