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BAYER DIAGNOSTICS ACS:180 AND ADVIA CENTAUR ANTI-TPO ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003291
510(k) Type
Traditional
Applicant
BAYER DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2000
Days to Decision
46 days
Submission Type
Summary

BAYER DIAGNOSTICS ACS:180 AND ADVIA CENTAUR ANTI-TPO ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003291
510(k) Type
Traditional
Applicant
BAYER DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2000
Days to Decision
46 days
Submission Type
Summary