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BRAEMAR CARDIOKEY HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K130294
510(k) Type
Special
Applicant
Braemar Manufacturing, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2013
Days to Decision
252 days
Submission Type
Summary

BRAEMAR CARDIOKEY HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K130294
510(k) Type
Special
Applicant
Braemar Manufacturing, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2013
Days to Decision
252 days
Submission Type
Summary