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ACL SYSTEMS 100, 200, 300 AND 300+ COAGULATION SYS

Page Type
Cleared 510(K)
510(k) Number
K881367
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1988
Days to Decision
88 days

ACL SYSTEMS 100, 200, 300 AND 300+ COAGULATION SYS

Page Type
Cleared 510(K)
510(k) Number
K881367
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1988
Days to Decision
88 days