FDA device listing

B24P - 24lb Bi-Lateral Pulleys,B30P - 30lb Bi-Lateral Pulleys,B50P - 50lb Bi-lateral Pulleys,B65P - 65lb Bi-lateral…

FDA device listing 1489895911 · CARDON REHABILITATION AND MEDICAL EQUIPMENT

Key facts

Proprietary names B24P - 24lb Bi-Lateral Pulleys,B30P - 30lb Bi-Lateral Pulleys,B50P - 50lb Bi-lateral Pulleys,B65P - 65lb Bi-lateral Pulleys,Corner Training Stand,L107P - 107lb Lateral Pulley,L177P - 177lb Lateral pulley,M100S - 220lb Speed Pulley,M24MP - 24lb Mobile Pulley,M30MP -30lb Mobile Pulley,M30SMP -30lb Mobile Speed Pulley,M60S - 132lb Speed Pulley,Mobile Suspension Frame,MPPB - Multi-Purpose Pulley…
Owner/operator CARDON REHABILITATION AND MEDICAL EQUIPMENT
Owner/operator number 9103979
Product codes ION
Device names ION - Exerciser, Non-Measuring
Device class Class I
Classification regulations (21 CFR) 890.5370
Review panels Physical Medicine
Registered establishments CARDON REHABILITATION AND MEDICAL EQUIPMENT
Establishment registrations 3007028274
FEI numbers 3007028274
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings