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LIQUISPX LIQUID LIPID CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012855
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2001
Days to Decision
6 days
Submission Type
Statement

LIQUISPX LIQUID LIPID CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012855
510(k) Type
Traditional
Applicant
CLINICAL CONTROLS DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2001
Days to Decision
6 days
Submission Type
Statement