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Eko Electronic Stethoscope System

Page Type
Cleared 510(K)
510(k) Number
K151319
510(k) Type
Traditional
Applicant
Eko Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2015
Days to Decision
102 days
Submission Type
Statement

Eko Electronic Stethoscope System

Page Type
Cleared 510(K)
510(k) Number
K151319
510(k) Type
Traditional
Applicant
Eko Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2015
Days to Decision
102 days
Submission Type
Statement