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IONTOPHORESIS DEVICE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K914621
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
12/20/1991
Days to Decision
100 days
Submission Type
Statement

IONTOPHORESIS DEVICE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K914621
510(k) Type
Traditional
Applicant
IOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
12/20/1991
Days to Decision
100 days
Submission Type
Statement