Last synced on 6 June 2025 at 11:06 pm

ABUSCREEN RADIOIMMUNOASSAY FOR METHAMPHETAMINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894465
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1989
Days to Decision
26 days

ABUSCREEN RADIOIMMUNOASSAY FOR METHAMPHETAMINE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894465
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1989
Days to Decision
26 days