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DELFIA (TM) HCG KIT

Page Type
Cleared 510(K)
510(k) Number
K862044
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1986
Days to Decision
44 days

DELFIA (TM) HCG KIT

Page Type
Cleared 510(K)
510(k) Number
K862044
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/1986
Days to Decision
44 days