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ACL COAGULATION SYSTEMS,MODELS 1000,2000,3000,PLUS

Page Type
Cleared 510(K)
510(k) Number
K912087
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1991
Days to Decision
129 days
Submission Type
Statement

ACL COAGULATION SYSTEMS,MODELS 1000,2000,3000,PLUS

Page Type
Cleared 510(K)
510(k) Number
K912087
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1991
Days to Decision
129 days
Submission Type
Statement