Last synced on 14 November 2025 at 11:06 pm

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE

Page Type
Cleared 510(K)
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)
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