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DYNATRON IBOX IONTOPHORESIS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K043047
510(k) Type
Traditional
Applicant
DYNATRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
1/7/2005
Days to Decision
64 days
Submission Type
Summary

DYNATRON IBOX IONTOPHORESIS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K043047
510(k) Type
Traditional
Applicant
DYNATRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
1/7/2005
Days to Decision
64 days
Submission Type
Summary