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TRIVARION BUFFERED IONTOPHORESIS ELECTRODE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061522
510(k) Type
Traditional
Applicant
ACTIVA TEK INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2006
Days to Decision
60 days
Submission Type
Summary

TRIVARION BUFFERED IONTOPHORESIS ELECTRODE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061522
510(k) Type
Traditional
Applicant
ACTIVA TEK INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2006
Days to Decision
60 days
Submission Type
Summary