De Novo

DEN070006: BINAX NOW MALARIA TEST; MODEL 660-000, 660-XXX

FDA De Novo · inverness medical professional diagnostics-binax · decided Jun 13, 2007

Key facts

De Novo number DEN070006
Device name BINAX NOW MALARIA TEST; MODEL 660-000, 660-XXX
Applicant inverness medical professional diagnostics-binax
Product code OAX
Date received Mar 23, 2007
Decision date Jun 13, 2007
Decision granted (DENG)
FDA classification Class II
Review panel Microbiology

At a glance

  • None 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:

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