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BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720

Page Type
Cleared 510(K)
510(k) Number
K981394
510(k) Type
Traditional
Applicant
BRAEMAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1998
Days to Decision
164 days
Submission Type
Summary

BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720

Page Type
Cleared 510(K)
510(k) Number
K981394
510(k) Type
Traditional
Applicant
BRAEMAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1998
Days to Decision
164 days
Submission Type
Summary