Last synced on 6 June 2025 at 11:06 pm

ABUSCREEN(R) ONTRAK(TM) FOR AMPHETAMINE(500 NG/ML)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910278
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1991
Days to Decision
70 days

ABUSCREEN(R) ONTRAK(TM) FOR AMPHETAMINE(500 NG/ML)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910278
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1991
Days to Decision
70 days