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MODEL MICRO SI AMBULATORY ECG MONITOR

Page Type
Cleared 510(K)
510(k) Number
K881905
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1988
Days to Decision
88 days

MODEL MICRO SI AMBULATORY ECG MONITOR

Page Type
Cleared 510(K)
510(k) Number
K881905
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1988
Days to Decision
88 days