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QUINTON Q, SCAN MODELS 900 & 901

Page Type
Cleared 510(K)
510(k) Number
K821758
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1982
Days to Decision
71 days

QUINTON Q, SCAN MODELS 900 & 901

Page Type
Cleared 510(K)
510(k) Number
K821758
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1982
Days to Decision
71 days