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USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932318
510(k) Type
Traditional
Applicant
U.S. DRUG TESTING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1993
Days to Decision
35 days
Submission Type
Statement

USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932318
510(k) Type
Traditional
Applicant
U.S. DRUG TESTING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1993
Days to Decision
35 days
Submission Type
Statement