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ACL AcuStar

Page Type
Cleared 510(K)
510(k) Number
K170314
510(k) Type
Special
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2017
Days to Decision
30 days
Submission Type
Summary

ACL AcuStar

Page Type
Cleared 510(K)
510(k) Number
K170314
510(k) Type
Special
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2017
Days to Decision
30 days
Submission Type
Summary