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LIAISON XL HCG

Page Type
Cleared 510(K)
510(k) Number
K131037
510(k) Type
Traditional
Applicant
DIASORIN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2013
Days to Decision
144 days
Submission Type
Summary

LIAISON XL HCG

Page Type
Cleared 510(K)
510(k) Number
K131037
510(k) Type
Traditional
Applicant
DIASORIN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2013
Days to Decision
144 days
Submission Type
Summary