← Back to catalogue
Acclarent Aera Eustachian Tube Balloon Dilation System
FDA 510(k)Class II (US FDA 510(k))
510(k) DEN150056
Identifiers
- 510(k) Number
- DEN150056 FDA 510(k)
- FDA Product Code
- PNZ FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 874.4180 FDA 510(k)
- Regulation Number
- 874.4180 FDA 510(k)
- Advisory Committee
- Ear, Nose, Throat FDA 510(k)
- FDA Decision
- DENG FDA 510(k)
Acclarent Aera Eustachian Tube Balloon Dilation System by Acclarent, Inc. — Class II — 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 | DEN150056 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Acclarent, Inc.
Sources (1)
- FDA 510(k) DEN150056 24 fields · synced Jun 18, 2026