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MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060236
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2006
Days to Decision
60 days
Submission Type
Summary

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060236
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2006
Days to Decision
60 days
Submission Type
Summary