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ARRHYTHMIA PROGRAM MODULE

Page Type
Cleared 510(K)
510(k) Number
K780432
510(k) Type
Traditional
Applicant
MIDWEST ANALOG & DIGITAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1978
Days to Decision
70 days

ARRHYTHMIA PROGRAM MODULE

Page Type
Cleared 510(K)
510(k) Number
K780432
510(k) Type
Traditional
Applicant
MIDWEST ANALOG & DIGITAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1978
Days to Decision
70 days