Last synced on 25 January 2026 at 3:41 am

ImmuLisa Enhanced RF IgA Antibody ELISA, ImmuLisa Enhanced RF IgG Antibody ELISA, ImmuLisa Enhanced RF IgM Antibody ELISA, ImmuLisa Enhanced RF Antibody Screen ELISA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143736
510(k) Type
Traditional
Applicant
Immco Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2015
Days to Decision
267 days
Submission Type
Statement

ImmuLisa Enhanced RF IgA Antibody ELISA, ImmuLisa Enhanced RF IgG Antibody ELISA, ImmuLisa Enhanced RF IgM Antibody ELISA, ImmuLisa Enhanced RF Antibody Screen ELISA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143736
510(k) Type
Traditional
Applicant
Immco Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2015
Days to Decision
267 days
Submission Type
Statement