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DIRECT LDL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981303
510(k) Type
Traditional
Applicant
Abbott Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1998
Days to Decision
115 days
Submission Type
Summary

DIRECT LDL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981303
510(k) Type
Traditional
Applicant
Abbott Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1998
Days to Decision
115 days
Submission Type
Summary