Source document or public record
FDA 510(k) K234088 — Emily's Care Nourish Test System (Model 1)
FDA 510(k) index record K234088. Device: Emily's Care Nourish Test System (Model 1). Applicant as listed: Lactation Lab, Inc.. Decision date: 2024-05-03.
Source
"device_name": "Emily's Care Nourish Test System (Model 1)"
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 K234088.
Device name: Emily's Care Nourish Test System (Model 1). Applicant as listed: Lactation Lab, Inc..
Decision date: 2024-05-03. Decision wording: Substantially Equivalent.
Product code: QEI. Regulation: 21 CFR 862.1493. Medical specialty: Clinical Chemistry.
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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