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Vivo 200 Dps Vivoscan Version 2.0 Oae Audiometer
FDA 510(k)Class II (US FDA 510(k))
510(k) K033108
Identifiers
- 510(k) Number
- K033108 FDA 510(k)
- FDA Product Code
- EWO FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 874.1050 FDA 510(k)
- Regulation Number
- 874.1050 FDA 510(k)
- Advisory Committee
- Ear, Nose, Throat FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Vivo 200 Dps Vivoscan Version 2.0 Oae Audiometer by Vivosonic 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 | K033108 | Class II | Active |
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Manufacturer
- Manufacturer
- Vivosonic Inc
- FDA Applicant
- Vivosonic, Inc.
Sources (1)
- FDA 510(k) K033108 24 fields · synced Jun 18, 2026