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Drt4 Laser Doppler Perfusion And Temperature Monitor
FDA 510(k)Class II (US FDA 510(k))
510(k) K011070
Identifiers
- 510(k) Number
- K011070 FDA 510(k)
- FDA Product Code
- GEX FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4810 FDA 510(k)
- Regulation Number
- 878.4810 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Drt4 Laser Doppler Perfusion And Temperature Monitor by Moor Instruments Ltd — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Manufacturer's product page: Laser Speckle Blood Flow and Tissue Oxygenation Imager
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 | K011070 | Class II | Active |
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Manufacturer
- Manufacturer
- Moor Instruments Ltd
- FDA Applicant
- Moor Instruments, Ltd.
Sources (1)
- FDA 510(k) K011070 24 fields · synced Jun 18, 2026