510(k) Report

FDA applicant

Dpcom AS

Ne, MN1 decision2010–20100 recalls

FDA records 1 decision for Dpcom AS (Ne, MN) in 2010: 1 510(k) clearance. All are in product code GWM (Device, Monitoring, Intracranial Pressure). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Dpcom AS’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Dpcom AS by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GWMDevice, Monitoring, Intracranial Pressure1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K101133Sensometrics SoftwareDpcom AS · 2010

The one decision as Dpcom AS →