← Back to catalogue
Immulisa Celiac G+ (gliadin) Iga And Igg Antibody Elisa
FDA 510(k)Class II (US FDA 510(k))
510(k) K091522
Identifiers
- 510(k) Number
- K091522 FDA 510(k)
- FDA Product Code
- MST FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 866.5750 FDA 510(k)
- Regulation Number
- 866.5750 FDA 510(k)
- Advisory Committee
- Immunology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Immulisa Celiac G+ (gliadin) Iga And Igg Antibody Elisa by Immco Diagnostics, Inc. — 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 | K091522 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Immco Diagnostics, Inc.
Sources (1)
- FDA 510(k) K091522 24 fields · synced Oct 6, 2026