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ADVIA 2120 WITH AUTOSLIDE SYSTEM, AND ADVIA 2120I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102644
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2011
Days to Decision
435 days
Submission Type
Summary

ADVIA 2120 WITH AUTOSLIDE SYSTEM, AND ADVIA 2120I

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102644
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2011
Days to Decision
435 days
Submission Type
Summary