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DIGITAL TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL EV-803 DIGITAL TENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020749
510(k) Type
Abbreviated
Applicant
EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2002
Days to Decision
238 days
Submission Type
Summary

DIGITAL TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL EV-803 DIGITAL TENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020749
510(k) Type
Abbreviated
Applicant
EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2002
Days to Decision
238 days
Submission Type
Summary