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KC 40 MICRO COAGULATION ANALYZER SYSTEM (K3632)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960875
510(k) Type
Traditional
Applicant
SIGMA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1996
Days to Decision
190 days
Submission Type
Summary

KC 40 MICRO COAGULATION ANALYZER SYSTEM (K3632)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960875
510(k) Type
Traditional
Applicant
SIGMA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1996
Days to Decision
190 days
Submission Type
Summary