Last synced on 14 November 2025 at 11:06 pm

CHOLESTECH L.D.X. LIPID ANALYZER, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K911578
510(k) Type
Traditional
Applicant
CHOLESTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1991
Days to Decision
49 days

CHOLESTECH L.D.X. LIPID ANALYZER, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K911578
510(k) Type
Traditional
Applicant
CHOLESTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1991
Days to Decision
49 days