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VenSure Balloon Device, VenSure Nav Balloon Device
FDA 510(k)Class I (US FDA 510(k))
510(k) K201472
by Fiagon GmbH
Identifiers
- 510(k) Number
- K201472 FDA 510(k)
- FDA Product Code
- LRC FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 874.4420 FDA 510(k)
- Regulation Number
- 874.4420 FDA 510(k)
- Advisory Committee
- Ear, Nose, Throat FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
VenSure Balloon Device, VenSure Nav Balloon Device by Fiagon GmbH — Class I — FDA_510K — listed in FDA 510(k) — 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 | K201472 | Class I | Active |
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Manufacturer
- Manufacturer
- Fiagon GmbH
Sources (1)
- FDA 510(k) K201472 24 fields · synced Jun 18, 2026