De Novo

DEN180007: Miris Human Milk Analyzer

FDA De Novo · miris ab · decided Dec 21, 2018

Key facts

De Novo number DEN180007
Device name Miris Human Milk Analyzer
Applicant miris ab
Product code QEI
Date received Feb 12, 2018
Decision date Dec 21, 2018
Decision granted (DENG)
FDA classification Class II
Review panel Clinical Chemistry
FEI number 3013887826

At a glance

  • 1–9 Later 510(k)s citing this De Novo
  • 1–9 UDI device identifiers (GUDID)
  • None MAUDE adverse event reports
  • None Recall events
  • No Decision summary on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About De Novo classification requests

The De Novo pathway classifies novel low- to moderate-risk devices that have no legally marketed predicate; each granted request creates a new classification regulation and product code.

Source: U.S. Food and Drug Administration (FDA), De Novo database · Source date:

Browse all De Novo classification requests