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ECG MONITORING SYSTEM,

Page Type
Cleared 510(K)
510(k) Number
K780404
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1978
Days to Decision
15 days

ECG MONITORING SYSTEM,

Page Type
Cleared 510(K)
510(k) Number
K780404
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1978
Days to Decision
15 days