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LIGHT PEN ACCESSORY FOR USE WITH FETASCAN 800 SERIES

Page Type
Cleared 510(K)
510(k) Number
K827712
510(k) Type
Traditional
Applicant
CRANSTON MEDICAL LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
55 days

LIGHT PEN ACCESSORY FOR USE WITH FETASCAN 800 SERIES

Page Type
Cleared 510(K)
510(k) Number
K827712
510(k) Type
Traditional
Applicant
CRANSTON MEDICAL LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
55 days