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BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER

Page Type
Cleared 510(K)
510(k) Number
K072008
510(k) Type
Traditional
Applicant
BRAEMAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2007
Days to Decision
72 days
Submission Type
Statement

BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER

Page Type
Cleared 510(K)
510(k) Number
K072008
510(k) Type
Traditional
Applicant
BRAEMAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2007
Days to Decision
72 days
Submission Type
Statement