QEI · Breast Milk Macronutrients Test System

Clinical Chemistry · 21 CFR 862.1493 · Class 2

Overview

Product CodeQEI
Device NameBreast Milk Macronutrients Test System
Regulation21 CFR 862.1493
Device ClassClass 2
Review PanelClinical Chemistry

Identification

A breast milk macronutrients test system is a device intended to quantitatively measure fat, protein, and total carbohydrate content in human breast milk. These measurements, in conjunction with other clinical assessments, may be used to aid in the nutritional management of infants.

Classification Rationale

Class II (special controls). The special controls for this device are:

Special Controls

A breast milk macronutrient test system must comply with the following special controls:

*Classification.* Class II (special controls). The special controls for this device are:(1) Design verification and validation must include the following: (i) An appropriate traceability plan, as determined by FDA, to minimize the risk of drift in the breast milk macronutrient test system results over time. (ii) Data that demonstrate appropriate precision, as determined by FDA, of the breast milk macronutrients test system. Precision studies must include assessment of a minimum of three breast milk specimens containing different concentrations (low, medium, and high levels) of fat, carbohydrates, and protein. Precision data must include breast milk specimen measurements that are collected at a minimum of three laboratory sites. (iii) Data that demonstrate appropriate measurement accuracy, as determined by FDA, of fat, carbohydrates, and protein in breast milk. Measurement accuracy data must include breast milk specimen measurements that are collected at a minimum of one laboratory site. (iv) Data from studies appropriate, as determined by FDA, to demonstrate that the device is free from significant interference from substances that could be present in human milk, including hemoglobin, and medications that are used by breastfeeding subjects. (2) The labeling required under § 809.10 of this chapter must include a limiting statement indicating that the results should be used only as an aid in the nutritional management of infants and not as the sole basis for making nutrition decisions.

Recent Cleared Devices (3 of 3)

RecordDevice NameApplicantDecision DateDecision
K234088Emily's Care Nourish Test System (Model 1)Lactation Lab, Inc.May 3, 2024SESE
K223085Miris Human Milk Analyzer (HMA)Miris ABSep 29, 2023SESE
DEN180007Miris Human Milk AnalyzerMiris ABDec 21, 2018DENG

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