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FIBRIN ANALYSIS SYSTEM ENDOLUMINAL BRUSH

Page Type
Cleared 510(K)
510(k) Number
K050889
510(k) Type
Traditional
Applicant
CRS MEDICAL DIAGNOSTICS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2005
Days to Decision
142 days
Submission Type
Summary

FIBRIN ANALYSIS SYSTEM ENDOLUMINAL BRUSH

Page Type
Cleared 510(K)
510(k) Number
K050889
510(k) Type
Traditional
Applicant
CRS MEDICAL DIAGNOSTICS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2005
Days to Decision
142 days
Submission Type
Summary