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DELFIA TM HLH KIT

Page Type
Cleared 510(K)
510(k) Number
K855173
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1986
Days to Decision
64 days

DELFIA TM HLH KIT

Page Type
Cleared 510(K)
510(k) Number
K855173
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1986
Days to Decision
64 days