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Relieva Seeker Balloon Sinuplasty System
FDA 510(k)Class I (US FDA 510(k))
510(k) K120280
Identifiers
- 510(k) Number
- K120280 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)
Relieva Seeker Balloon Sinuplasty System by Acclarent, Inc. — 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 | K120280 | Class I | Active |
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Manufacturer
- Manufacturer
- Acclarent, Inc.
Sources (1)
- FDA 510(k) K120280 24 fields · synced Jun 18, 2026