# Robert R. Moore

- Location (FDA's records): Walker, MI
- FDA decisions: 5 (1977–1977): 5 510(k) clearances
- Product codes: ION (1), IPM (1), KPR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K770658: Exerciser, Leg, Lower Extremity (Jun 17, 1977)
- K770501: Knee Cuff for Expressing Fluid (Apr 5, 1977)
- K770223: Heavy Foam Heel & Elbow Protectors (Feb 23, 1977)
- K770060: X-Ray Positioning Device (Jan 24, 1977)
- K770059: Orthopedic Specialties (Jan 14, 1977)

Source page: https://510kreport.com/company/robert-r-moore