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ACL 9000 SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000053
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2000
Days to Decision
68 days
Submission Type
Summary

ACL 9000 SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000053
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2000
Days to Decision
68 days
Submission Type
Summary