510(k) Report

FDA applicant

Robert R. Moore

Walker, MI5 decisions1977–19770 recalls

FDA records 5 decisions for Robert R. Moore (Walker, MI) in 1977: 5 510(k) clearances. Most are in product codes ION (Exerciser, Non-Measuring) and IPM (Cover, Limb). 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 Robert R. Moore’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Robert R. Moore since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Robert R. Moore 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?

  • IONExerciser, Non-Measuring1decision
  • IPMCover, Limb1decision
  • KPRSystem, X-Ray, Stationary1decision

What has FDA decided for it lately?

  • K770658Exerciser, Leg, Lower ExtremityRobert R. Moore · 1977
  • K770501Knee Cuff for Expressing FluidRobert R. Moore · 1977
  • K770223Heavy Foam Heel & Elbow ProtectorsRobert R. Moore · 1977
  • K770060X-Ray Positioning DeviceRobert R. Moore · 1977
  • K770059Orthopedic SpecialtiesRobert R. Moore · 1977

All 5 as Robert R. Moore →

Other applicant names beginning “Robert”

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

Robert Bosch Corp. 21Robert I. Chien & Assoc., Inc. 6Robert W. Bauer & Assoc., Inc. 3Robert A James 2Robert R. Stevens 2Robert Reid, Inc. 2Robert B. Scott Ocularists of Florida, Inc. 2Robert J. Sislian, Inc. 1Robert C. Cameron 1Robert Shaw Controls Co. 1Robert C. Leif, Ph.D. 1Robert Bosch Healthcare Systems, Inc. 1