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HEMOSIL INR VALIDATE, HEMOSIL ISI CALIBRATE, ISIWEB (SOFTWARE)

Page Type
Cleared 510(K)
510(k) Number
K090563
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2009
Days to Decision
221 days
Submission Type
Summary

HEMOSIL INR VALIDATE, HEMOSIL ISI CALIBRATE, ISIWEB (SOFTWARE)

Page Type
Cleared 510(K)
510(k) Number
K090563
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/2009
Days to Decision
221 days
Submission Type
Summary