Source document or public record
FDA 510(k) K230944 — MeMed BV
FDA 510(k) index record K230944. Device: MeMed BV. Applicant as listed: MeMed Diagnostics, Ltd.. Decision date: 2023-06-30.
Source
"device_name": "MeMed BV"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K230944.
Device name: MeMed BV. Applicant as listed: MeMed Diagnostics, Ltd..
Decision date: 2023-06-30. Decision wording: Substantially Equivalent.
Product code: QPS. Regulation: 21 CFR 866.3215. 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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