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ABUSCREEN(R) ONTRAK(TM) FOR THC

Page Type
Cleared 510(K)
510(k) Number
K881814
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1988
Days to Decision
92 days

ABUSCREEN(R) ONTRAK(TM) FOR THC

Page Type
Cleared 510(K)
510(k) Number
K881814
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1988
Days to Decision
92 days