FDA device listing
X100HT with Full Field Peripheral Blood Smear (PBS) Application
FDA device listing 1803848227 · Scopio Labs Ltd.
Key facts
| Proprietary names | X100HT with Full Field Peripheral Blood Smear (PBS) Application |
|---|---|
| Owner/operator | Scopio Labs Ltd. |
| Owner/operator number | 10080474 |
| Premarket submissions | K220013 |
| Product codes | JOY |
| Device names | JOY - Device, Automated Cell-Locating |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.5260 |
| Review panels | Hematology |
| Registered establishments | SCOPIO LABS LTD. |
| Establishment registrations | 3018182832 |
| FEI numbers | 3018182832 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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