FDA device listing
AMREX CB95 IF250 INTERFERENTIAL AND U/50 ULTRASOUND COMBINATION,AMREX SYCHROSONIC US/752 COMBINATION ULTRASOUND/HIGH…
FDA device listing 1207696033 · AMREX-ZETRON, INC.
Key facts
| Proprietary names | AMREX CB95 IF250 INTERFERENTIAL AND U/50 ULTRASOUND COMBINATION,AMREX SYCHROSONIC US/752 COMBINATION ULTRASOUND/HIGH VOLT PULSED DC STIMULATOR,AMREX SYNCHROSONIC U/HVG50 COMBINATION ULTRASOUND/ LOW VOLTAGE GALVANIC/HIGH VOLT STIMULATOR,AMREX SYNCHROSONIC US/50 COMBINATION ULTRASOUND / LOW VOLT AC STIMULATOR,AMREX SYNCHROSONIC US/54 COMBINATION ULTRASOUND / LOW VOLT AC… |
|---|---|
| Owner/operator | AMREX-ZETRON, INC. |
| Owner/operator number | 2011115 |
| Product codes | IMG |
| Device names | IMG - Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.5860 |
| Review panels | Physical Medicine |
| Registered establishments | AMREX-ZETRON, INC. |
| Establishment registrations | 2011115 |
| FEI numbers | 2011115 |
| 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