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MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K873680
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1987
Days to Decision
70 days

MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K873680
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1987
Days to Decision
70 days