510(k) Report

FDA applicant

Wrm Computers

Holland, HN2 decisions1992–19920 recalls

FDA records 2 decisions for Wrm Computers (Holland, HN) in 1992: 2 510(k) clearances. Most are in product codes IKE (Transducer, Miniature Pressure) and JFC (System, Pressure Measurement, Intermittent). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Wrm Computers since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wrm Computers by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IKETransducer, Miniature Pressure1decision
  • JFCSystem, Pressure Measurement, Intermittent1decision

What has FDA decided for it lately?

  • K915897FPLWrm Computers · 1992
  • K915278CDG Gait Analyses SystemWrm Computers · 1992

All 2 as Wrm Computers →