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ABUSCREEN RADIOIMMUNOASSAY FOR CANNABINIODS

Page Type
Cleared 510(K)
510(k) Number
K912757
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1991
Days to Decision
35 days
Submission Type
Statement

ABUSCREEN RADIOIMMUNOASSAY FOR CANNABINIODS

Page Type
Cleared 510(K)
510(k) Number
K912757
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1991
Days to Decision
35 days
Submission Type
Statement