510(k) Report

FDA applicant

Old Delft Corp. of America

Fairfax, VA3 decisions1986–19860 recalls

FDA records 3 decisions for Old Delft Corp. of America (Fairfax, VA) in 1986: 3 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and KPZ (Generator, High Voltage, X-Ray, Therapeutic). 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, radiology panel, where it files most

How often FDA has decided Old Delft Corp. of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Old Delft Corp. of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Old Delft Corp. of America 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?

  • KPRSystem, X-Ray, Stationary1decision
  • KPZGenerator, High Voltage, X-Ray, Therapeutic1decision
  • JADSystem, Therapeutic, X-Ray1decision

What has FDA decided for it lately?

  • K862616Amber-ChestOld Delft Corp. of America · 1986
  • K861431Therapax HT 150TOld Delft Corp. of America · 1986
  • K854410VeriflexOld Delft Corp. of America · 1986

All 3 as Old Delft Corp. of America →