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LANCER HDL SEPARATION KIT

Page Type
Cleared 510(K)
510(k) Number
K790865
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1979
Days to Decision
52 days

LANCER HDL SEPARATION KIT

Page Type
Cleared 510(K)
510(k) Number
K790865
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1979
Days to Decision
52 days