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IONTOPHORESIS SYSTEM MODULE, DM 500

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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