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BRAEMAR ER700 SERIES AMBULATORY ECG EVENT MONITOR MODELS ER710,ER720

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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