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Q700 ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K864700
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1987
Days to Decision
79 days

Q700 ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K864700
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1987
Days to Decision
79 days