510(k) Report

FDA applicant

World Precision Instruments, Inc.

New Haven, CT2 decisions1985–19880 recalls

FDA records 2 decisions for World Precision Instruments, Inc. (New Haven, CT) from 1985 to 1988: 2 510(k) clearances. Most are in product codes GYA (Tester, Electrode/Lead, Electroencephalograph) and FFT (Electrode, Ph, Stomach). 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 World Precision Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for World Precision Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — World Precision Instruments, Inc. 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?

  • GYATester, Electrode/Lead, Electroencephalograph1decision
  • FFTElectrode, Ph, Stomach1decision

What has FDA decided for it lately?

  • K883869DermtrodeWorld Precision Instruments, Inc. · 1988
  • K852289Model SA3 Esophageal PH ElectrodeWorld Precision Instruments, Inc. · 1985

All 2 as World Precision Instruments, Inc. →