Identifiers
- 510(k) Number
- K092471 FDA 510(k)
- FDA Product Code
- IYX FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.1100 FDA 510(k)
- Regulation Number
- 892.1100 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Model Sentinella 102 by General Equipment For Medical Imaging, S.a. — Class I — MDR, FDA_510K — listed in FDA 510(k), EUDAMED — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
MDR
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Active |
| FDA 510(k) | United States | FDA_510K | K092471 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- General Equipment For Medical Imaging, S.a.
Sources (2)
- FDA 510(k) K092471 24 fields · synced Jun 19, 2026
- EUDAMED 1 fields · synced May 18, 2026