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ABUSCREEN FP FOR CANNABINOIDS

Page Type
Cleared 510(K)
510(k) Number
K890887
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1989
Days to Decision
23 days

ABUSCREEN FP FOR CANNABINOIDS

Page Type
Cleared 510(K)
510(k) Number
K890887
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1989
Days to Decision
23 days