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LIAISON ALDOSTERONE, LIAISON ALDOSTERONE CONTROL SET, LIAISON ALDOSTERONE CALIBRATION VERIFIERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130321
510(k) Type
Traditional
Applicant
DIASORIN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2013
Days to Decision
60 days
Submission Type
Summary

LIAISON ALDOSTERONE, LIAISON ALDOSTERONE CONTROL SET, LIAISON ALDOSTERONE CALIBRATION VERIFIERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130321
510(k) Type
Traditional
Applicant
DIASORIN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2013
Days to Decision
60 days
Submission Type
Summary