Identifiers
- 510(k) Number
- K172843 FDA 510(k)
- FDA Product Code
- KOI FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 868.2775 FDA 510(k)
- Regulation Number
- 868.2775 FDA 510(k)
- Advisory Committee
- Anesthesiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
TwitchView System by Blink Device Company — 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 | K172843 | Class II | Active |
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Manufacturer
- Manufacturer
- Blink Device Company
- FDA Applicant
- Blink Device Corporation
Sources (1)
- FDA 510(k) K172843 24 fields · synced Jun 18, 2026