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Acorn 3D Software - Acorn 3DP Model (AC-101-XX)
FDA 510(k)Class II (US FDA 510(k))
510(k) K252103
Identifiers
- 510(k) Number
- K252103 FDA 510(k)
- FDA Product Code
- QIH FDA 510(k)
- Models / Variants
- Acorn 3D Software (AC-SEG-4009) FDA 510(k)Acorn 3DP Model (AC-101-XX) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.2050 FDA 510(k)
- Regulation Number
- 892.2050 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Acorn 3D Software - Acorn 3DP Model (AC-101-XX) by Mighty Oak Medical — Class II — FDA_510K — listed in FDA 510(k) — 2 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 | K252103 | Class II | Active |
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Manufacturer
- Manufacturer
- Mighty Oak Medical
Sources (1)
- FDA 510(k) K252103 24 fields · synced Oct 9, 2026