← Back to catalogue
Abusign Doa 2, Doa, Coc/Thc, Doa2, Biosign Doa2, Coc/Thc
FDA 510(k)Class II (US FDA 510(k))
510(k) K952361
Identifiers
- 510(k) Number
- K952361 FDA 510(k)
- FDA Product Code
- DIO FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 862.3250 FDA 510(k)
- Regulation Number
- 862.3250 FDA 510(k)
- Advisory Committee
- Clinical Toxicology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Abusign Doa 2, Doa, Coc/Thc, Doa2, Biosign Doa2, Coc/Thc by Princeton Biomeditech Corp. — Class II — FDA_510K — listed in FDA 510(k)
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 | K952361 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Princeton Biomeditech Corp.
Sources (1)
- FDA 510(k) K952361 24 fields · synced Jun 18, 2026