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630C ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K863030
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1986
Days to Decision
101 days

630C ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K863030
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/1986
Days to Decision
101 days