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LIQUID SCINTILLATION COUNTER

Page Type
Cleared 510(K)
510(k) Number
K780179
510(k) Type
Traditional
Applicant
ROCHE MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1978
Days to Decision
20 days

LIQUID SCINTILLATION COUNTER

Page Type
Cleared 510(K)
510(k) Number
K780179
510(k) Type
Traditional
Applicant
ROCHE MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1978
Days to Decision
20 days