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Helena Plasminogen Quiplate Procedure
FDA 510(k)Class I (US FDA 510(k))
510(k) K811777
Identifiers
- 510(k) Number
- K811777 FDA 510(k)
- FDA Product Code
- DDX FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 866.5715 FDA 510(k)
- Regulation Number
- 866.5715 FDA 510(k)
- Advisory Committee
- Immunology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Helena Plasminogen Quiplate Procedure by Helena Laboratories — 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 | K811777 | Class I | Active |
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Manufacturer
- Manufacturer
- Helena Laboratories
Sources (1)
- FDA 510(k) K811777 24 fields · synced Jun 18, 2026