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DL900 SERIES HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K071733
510(k) Type
Special
Applicant
Braemar, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2007
Days to Decision
28 days
Submission Type
Statement

DL900 SERIES HOLTER RECORDER

Page Type
Cleared 510(K)
510(k) Number
K071733
510(k) Type
Special
Applicant
Braemar, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2007
Days to Decision
28 days
Submission Type
Statement