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CHIRON DIAGNOSTICS ACS: 180 FT3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991692
510(k) Type
Traditional
Applicant
CHIRON DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1999
Days to Decision
31 days
Submission Type
Summary

CHIRON DIAGNOSTICS ACS: 180 FT3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991692
510(k) Type
Traditional
Applicant
CHIRON DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1999
Days to Decision
31 days
Submission Type
Summary