Documento fuente o registro público
FDA 510(k) K232672 — EasyScreen Gastrointestinal Parasite Detection Kit
FDA 510(k) index record K232672. Device: EasyScreen Gastrointestinal Parasite Detection Kit. Applicant as listed: Genetic Signatures Limited. Decision date: 2024-05-29.
Fuente
"device_name": "EasyScreen Gastrointestinal Parasite Detection Kit"
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
Automated FDA record verification
2026-10-20
2026-10-27
professional use
FDA 510(k) public index record K232672.
Device name: EasyScreen Gastrointestinal Parasite Detection Kit. Applicant as listed: Genetic Signatures Limited.
Decision date: 2024-05-29. 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.
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