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LIQUID SCINTILLATION COUNTER

Page Type
Cleared 510(K)
510(k) Number
K790961
510(k) Type
Traditional
Applicant
NUCLEAR ENT. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1979
Days to Decision
37 days

LIQUID SCINTILLATION COUNTER

Page Type
Cleared 510(K)
510(k) Number
K790961
510(k) Type
Traditional
Applicant
NUCLEAR ENT. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1979
Days to Decision
37 days