Documento fuente o registro público

FDA 510(k) K203647 — SEFRIA Methamphetamine Oral Fluid Enzyme Immunoassay

FDA 510(k) index record K203647. Device: SEFRIA Methamphetamine Oral Fluid Enzyme Immunoassay. Applicant as listed: Immunalysis Corporation. Decision date: 2021-12-22.

OtherU.S. Food and Drug Administration (FDA)2021-12-22

Fuente

"device_name": "SEFRIA Methamphetamine Oral Fluid Enzyme Immunoassay"

Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.

Review and references

Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-31

Disclaimer

professional use

FDA 510(k) public index record K203647.

Device name: SEFRIA Methamphetamine Oral Fluid Enzyme Immunoassay. Applicant as listed: Immunalysis Corporation.

Decision date: 2021-12-22. Decision wording: Substantially Equivalent.

Product code: LAF. Regulation: 21 CFR 862.3610. Medical specialty: Clinical Toxicology.

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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