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ACL TOP 700 LAS

Page Type
Cleared 510(K)
510(k) Number
K091980
510(k) Type
Special
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2009
Days to Decision
83 days
Submission Type
Summary

ACL TOP 700 LAS

Page Type
Cleared 510(K)
510(k) Number
K091980
510(k) Type
Special
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2009
Days to Decision
83 days
Submission Type
Summary