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EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110509
510(k) Type
Traditional
Applicant
EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2011
Days to Decision
118 days
Submission Type
Summary

EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110509
510(k) Type
Traditional
Applicant
EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2011
Days to Decision
118 days
Submission Type
Summary