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Is-Toxoplasma Igg Test System
FDA 510(k)Class II (US FDA 510(k))
510(k) K981498
Identifiers
- 510(k) Number
- K981498 FDA 510(k)
- FDA Product Code
- LGD FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 866.3780 FDA 510(k)
- Regulation Number
- 866.3780 FDA 510(k)
- Advisory Committee
- Microbiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Is-Toxoplasma Igg Test System by Diamedix Corp. — Class II — 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 | K981498 | Class II | Active |
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Manufacturer
- Manufacturer
- Diamedix Corp.
Sources (1)
- FDA 510(k) K981498 24 fields · synced Jun 18, 2026