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IL TEST(TM) DAT CALIBRATOR A( -)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913739
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1991
Days to Decision
21 days
Submission Type
Statement

IL TEST(TM) DAT CALIBRATOR A( -)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913739
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1991
Days to Decision
21 days
Submission Type
Statement