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ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD AND ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031759
510(k) Type
Special
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2003
Days to Decision
59 days
Submission Type
Summary

ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD AND ACON SPECTRUM MULTI-DRUG MULTI-LINE DRUG SCREEN TEST CARD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031759
510(k) Type
Special
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2003
Days to Decision
59 days
Submission Type
Summary