FDA device listing
Device, Pressure Applying
FDA device listing 2017606264 · Hansol Medical Co.
Key facts
| Owner/operator | Hansol Medical Co. |
|---|---|
| Owner/operator number | 9034494 |
| Product codes | KNM |
| Device names | KNM - Device, Pressure Applying |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5765 |
| Review panels | Physical Medicine |
| Registered establishments | HANSOL MEDICAL CO. |
| Establishment registrations | 3005417950 |
| FEI numbers | 3005417950 |
| Establishment operations | Contract Manufacturer, 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