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Eko Model E5 System (EME5), Eko DUO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170874
510(k) Type
Traditional
Applicant
Eko Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2017
Days to Decision
56 days
Submission Type
Statement

Eko Model E5 System (EME5), Eko DUO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170874
510(k) Type
Traditional
Applicant
Eko Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2017
Days to Decision
56 days
Submission Type
Statement