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TOXOPLASMA IGG IN-VITRO DIAGNOSTIC SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955760
510(k) Type
Traditional
Applicant
Bayer Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1996
Days to Decision
226 days
Submission Type
Summary

TOXOPLASMA IGG IN-VITRO DIAGNOSTIC SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955760
510(k) Type
Traditional
Applicant
Bayer Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1996
Days to Decision
226 days
Submission Type
Summary