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DELFIA(TM) HIGE KIT

Page Type
Cleared 510(K)
510(k) Number
K871599
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1987
Days to Decision
49 days

DELFIA(TM) HIGE KIT

Page Type
Cleared 510(K)
510(k) Number
K871599
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1987
Days to Decision
49 days