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ER800 SERIES ECG EVENT RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030856
510(k) Type
Special
Applicant
BRAEMAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
10 days
Submission Type
Summary

ER800 SERIES ECG EVENT RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030856
510(k) Type
Special
Applicant
BRAEMAR CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
10 days
Submission Type
Summary