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Q4000 AND Q3040 ELECTROCARDIOGRAPH MONITOR

Page Type
Cleared 510(K)
510(k) Number
K863159
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1986
Days to Decision
49 days

Q4000 AND Q3040 ELECTROCARDIOGRAPH MONITOR

Page Type
Cleared 510(K)
510(k) Number
K863159
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1986
Days to Decision
49 days