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IL TEST(TM) PRO-CHROM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924884
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1993
Days to Decision
108 days
Submission Type
Summary

IL TEST(TM) PRO-CHROM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924884
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1993
Days to Decision
108 days
Submission Type
Summary