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Everyway Incontinence Stimulation System

Page Type
Cleared 510(K)
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)
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