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IGX PLEX RHEUMATOID ARTHRITIS (RA) ASSAY AND SQIDWORKS DIAGNOSTICS PLATFORM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083080
510(k) Type
Traditional
Applicant
SQI DIAGNOSTICS SYSTEMS
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/29/2009
Days to Decision
378 days
Submission Type
Summary

IGX PLEX RHEUMATOID ARTHRITIS (RA) ASSAY AND SQIDWORKS DIAGNOSTICS PLATFORM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083080
510(k) Type
Traditional
Applicant
SQI DIAGNOSTICS SYSTEMS
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
10/29/2009
Days to Decision
378 days
Submission Type
Summary