510(k) Report

FDA applicant

Rich-Larky Company, Inc.

Washington, DC1 decision1985–19850 recalls

FDA records 1 decision for Rich-Larky Company, Inc. (Washington, DC) in 1985: 1 510(k) clearance. All are in product code HOX (Chart, Visual Acuity). 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, ophthalmic panel, where it files most

How often FDA has decided Rich-Larky Company, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rich-Larky Company, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rich-Larky Company, 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?

  • HOXChart, Visual Acuity1decision

What has FDA decided for it lately?

  • K854047IN-Home Vision Monitoring KitRich-Larky Company, Inc. · 1985

The one decision as Rich-Larky Company, Inc. →

Other applicant names beginning “Rich-Larky”

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

Rich-Mar Corp. 43Rich Mountain Medical Products, Inc. 7