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QUINTON MODEL 630 AND 636 ECG DATA CART

Page Type
Cleared 510(K)
510(k) Number
K791364
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1979
Days to Decision
24 days

QUINTON MODEL 630 AND 636 ECG DATA CART

Page Type
Cleared 510(K)
510(k) Number
K791364
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1979
Days to Decision
24 days