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IONTOPHORESIS SYSTEM MODULE, DM 500

Page Type
Cleared 510(K)
510(k) Number
K770717
510(k) Type
Traditional
Applicant
SORENSEN RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1977
Days to Decision
119 days

IONTOPHORESIS SYSTEM MODULE, DM 500

Page Type
Cleared 510(K)
510(k) Number
K770717
510(k) Type
Traditional
Applicant
SORENSEN RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1977
Days to Decision
119 days