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PRESSON ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K121347
510(k) Type
Traditional
Applicant
Rhythmlink International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2012
Days to Decision
72 days
Submission Type
Statement

PRESSON ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K121347
510(k) Type
Traditional
Applicant
Rhythmlink International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2012
Days to Decision
72 days
Submission Type
Statement