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QUINTON MODEL 530X ECG DATA CART

Page Type
Cleared 510(K)
510(k) Number
K790739
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1979
Days to Decision
10 days

QUINTON MODEL 530X ECG DATA CART

Page Type
Cleared 510(K)
510(k) Number
K790739
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1979
Days to Decision
10 days