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AMBULATORY MONITORING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K833162
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1984
Days to Decision
116 days

AMBULATORY MONITORING DEVICE

Page Type
Cleared 510(K)
510(k) Number
K833162
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1984
Days to Decision
116 days