FDA device listing
PROEMG
FDA device listing 1566551344 · BIO PROTECH, INC.
Key facts
| Proprietary names | PROEMG |
|---|---|
| Owner/operator | BIO PROTECH, INC. |
| Owner/operator number | 9048345 |
| Premarket submissions | K152984 |
| Product codes | GXZ, IKT |
| Device names | GXZ - Electrode, Needle, IKT - Electrode, Needle, Diagnostic Electromyograph |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.1350, 890.1385 |
| Review panels | Neurology, Physical Medicine |
| Registered establishments | BIO PROTECH, INC., BIO PROTECH YANTAI INC |
| Establishment registrations | 9710582, 3010805941 |
| FEI numbers | 3003514332, 3010805941 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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