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Surevue Serum/Urine Hcg (1 +3 more)
FDA 510(k)Class II (US FDA 510(k))
510(k) K010593
Identifiers
- 510(k) Number
- K010593 FDA 510(k)
- FDA Product Code
- JHI FDA 510(k)
- Models / Variants
- 1 FDA 510(k)30 FDA 510(k)50 FDA 510(k)100 Test Kit FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 862.1155 FDA 510(k)
- Regulation Number
- 862.1155 FDA 510(k)
- Advisory Committee
- Clinical Chemistry FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Surevue Serum/Urine Hcg (1 +3 more) by Sa Scientific, Inc. — 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 | K010593 | Class II | Active |
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Manufacturer
- Manufacturer
- Sa Scientific, Inc.
Sources (1)
- FDA 510(k) K010593 24 fields · synced Jun 18, 2026