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MODEL MICRO FD+ AMBULATORY ECG MONITOR

Page Type
Cleared 510(K)
510(k) Number
K872508
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1987
Days to Decision
93 days

MODEL MICRO FD+ AMBULATORY ECG MONITOR

Page Type
Cleared 510(K)
510(k) Number
K872508
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1987
Days to Decision
93 days