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SCINTILLATION, LIQUID, RACKBETA

Page Type
Cleared 510(K)
510(k) Number
K780341
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1978
Days to Decision
86 days

SCINTILLATION, LIQUID, RACKBETA

Page Type
Cleared 510(K)
510(k) Number
K780341
510(k) Type
Traditional
Applicant
LKB INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1978
Days to Decision
86 days