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ABUSCREEN(R) ONLINE(TM) FOR AMPHETAMINES, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921998
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1992
Days to Decision
33 days
Submission Type
Statement

ABUSCREEN(R) ONLINE(TM) FOR AMPHETAMINES, MODIFIED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921998
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1992
Days to Decision
33 days
Submission Type
Statement