← Back to catalogue
Ness L300 System Kit, Lef Model Lg3-5100 +2 more models
FDA 510(k)Class II (US FDA 510(k))
510(k) K122784
by Bioness Inc.
Identifiers
- 510(k) Number
- K122784 FDA 510(k)
- FDA Product Code
- GZI FDA 510(k)
- Models / Variants
- Ness L300 System Kit, Lef Model Lg3-5100 FDA 510(k)Ness L300 System Kit, Right Model Lg3-5000 FDA 510(k)Small Ness L300 System Kit, Right FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 882.5810 FDA 510(k)
- Regulation Number
- 882.5810 FDA 510(k)
- Advisory Committee
- Neurology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Ness L300 System Kit, Lef Model Lg3-5100 +2 more models by Bioness Inc. — Class II — FDA_510K — listed in FDA 510(k) — 3 models — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K122784 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bioness Inc.
- FDA Applicant
- Bioness, Inc.
Sources (1)
- FDA 510(k) K122784 24 fields · synced Jun 18, 2026