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DUPEL IONTOPHORESIS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K915444
510(k) Type
Traditional
Applicant
EMPI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1994
Days to Decision
953 days
Submission Type
Statement

DUPEL IONTOPHORESIS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K915444
510(k) Type
Traditional
Applicant
EMPI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/1994
Days to Decision
953 days
Submission Type
Statement