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Everyway Incontinence Stimulation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213116
510(k) Type
Traditional
Applicant
Everyway Medical Instruments Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/3/2021
Days to Decision
67 days
Submission Type
Statement

Everyway Incontinence Stimulation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213116
510(k) Type
Traditional
Applicant
Everyway Medical Instruments Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/3/2021
Days to Decision
67 days
Submission Type
Statement