FDA device listing
Prism Plasma
FDA device listing 1161320884 · NEOconcepts LLC
Key facts
| Proprietary names | Prism Plasma |
|---|---|
| Owner/operator | NEOconcepts LLC |
| Owner/operator number | 10085708 |
| Premarket submissions | K233760 |
| Product codes | QVJ |
| Device names | QVJ - Low Power Electrosurgical Devices For Skin Lesion Destruction |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4400 |
| Review panels | General & Plastic Surgery |
| Registered establishments | NEOCONCEPTS LLC |
| Establishment registrations | 3015227849 |
| FEI numbers | 3015227849 |
| Establishment operations | Complaint File Establishment |
| 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