510(k) Report

FDA applicant

Washington Regulatory Services

Ringoes, NJ3 decisions1989–19990 recalls

FDA records 3 decisions for Washington Regulatory Services (Ringoes, NJ) from 1989 to 1999: 3 510(k) clearances. Most are in product codes HIG (Insufflator, Hysteroscopic) and MQF (Catheter, Assisted Reproduction). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Washington Regulatory Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Washington Regulatory Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Washington Regulatory Services 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?

  • HIGInsufflator, Hysteroscopic1decision
  • MQFCatheter, Assisted Reproduction1decision
  • DQOCatheter, Intravascular, Diagnostic1decision

What has FDA decided for it lately?

  • K983604Intra-Uterine Transfer, Intra-Folopian TransferWashington Regulatory Services · 1999
  • K894259Register, a Disposable Hysterography CupulaWashington Regulatory Services · 1990
  • K882658Angioscope for Pulmonary Artery UseWashington Regulatory Services · 1989

All 3 as Washington Regulatory Services →

Other applicant names beginning “Washington”

FDA records each applicant name separately; these may or may not be the same firm.

Washington-Greene County Branch Pennsylvania Assoc 3Washington Biotechnology 1The Washington Group, Inc. 1Washington Biolab, Inc. 1