Source document or public record
FDA 510(k) K242498 — Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC
FDA 510(k) index record K242498. Device: Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC. Applicant as listed: Aicheck Biotech, Inc.. Decision date: 2024-10-01.
Source
"device_name": "Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC"
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 K242498.
Device name: Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC. Applicant as listed: Aicheck Biotech, Inc..
Decision date: 2024-10-01. Decision wording: Substantially Equivalent.
Product code: NFT. Regulation: 21 CFR 862.3100. 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.
Interested in these solutions?
Submit a sourcing request with the assays, volumes, and timeline of your own project.