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TOXOPLASMA IGM ASSAY FOR THE BAYER IMMUNO1 SYSTEM (IN VITRO DIAGNOSTIC SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971989
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1997
Days to Decision
146 days
Submission Type
Summary

TOXOPLASMA IGM ASSAY FOR THE BAYER IMMUNO1 SYSTEM (IN VITRO DIAGNOSTIC SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971989
510(k) Type
Traditional
Applicant
BAYER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/1997
Days to Decision
146 days
Submission Type
Summary