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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
K161349
510(k) Type
Traditional
Applicant
EVERYWAY MEDICAL INSTRUMENT CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
417 days
Submission Type
Summary

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
K161349
510(k) Type
Traditional
Applicant
EVERYWAY MEDICAL INSTRUMENT CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/7/2017
Days to Decision
417 days
Submission Type
Summary