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120V Neptune S Rover (0711-001-000) +3 more models
FDA 510(k)Class II (US FDA 510(k))
510(k) K222552
Identifiers
- 510(k) Number
- K222552 FDA 510(k)
- FDA Product Code
- JCX FDA 510(k)
- Models / Variants
- 120V Neptune S Rover (0711-001-000) FDA 510(k)V2 4-Port Manifold (0750-400-000) FDA 510(k)V2 Specimen Collection Tray (0750-210-000) FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4780 FDA 510(k)
- Regulation Number
- 878.4780 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
120V Neptune S Rover (0711-001-000) +3 more models by Stryker Instruments — Class II — FDA_510K — listed in FDA 510(k) — 4 models — 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 | K222552 | Class II | Active |
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Manufacturer
- Manufacturer
- Stryker Instruments
Sources (1)
- FDA 510(k) K222552 24 fields · synced Jun 18, 2026