FDA device listing
No Proprietary Name
FDA device listing 1989414554 · Hypertec HCM LLC
Key facts
| Proprietary names | No Proprietary Name |
|---|---|
| Owner/operator | Hypertec HCM LLC |
| Owner/operator number | 10053193 |
| Premarket submissions | K191286 |
| Product codes | NBW |
| Device names | NBW - System, Test, Blood Glucose, Over The Counter |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1345 |
| Review panels | Clinical Chemistry |
| Registered establishments | Hypertec HCM LLC |
| Establishment registrations | 3013896610 |
| FEI numbers | 3013896610 |
| Establishment operations | Repackager/Relabeler |
| 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