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IONTOPHORESIS DEVICE - ELECTRODE RH 800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896444
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
5/10/1990
Days to Decision
182 days

IONTOPHORESIS DEVICE - ELECTRODE RH 800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896444
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
5/10/1990
Days to Decision
182 days