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IMMULISA CELIAC G+ (GLIADIN) IGA AND IGG ANTIBODY ELISA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091522
510(k) Type
Traditional
Applicant
Immco Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2010
Days to Decision
258 days
Submission Type
Statement

IMMULISA CELIAC G+ (GLIADIN) IGA AND IGG ANTIBODY ELISA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091522
510(k) Type
Traditional
Applicant
Immco Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2010
Days to Decision
258 days
Submission Type
Statement