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SOLARIS D890 THERAPY PROBE

Page Type
Cleared 510(K)
510(k) Number
K040729
510(k) Type
Traditional
Applicant
DYNATRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2004
Days to Decision
72 days
Submission Type
Summary

SOLARIS D890 THERAPY PROBE

Page Type
Cleared 510(K)
510(k) Number
K040729
510(k) Type
Traditional
Applicant
DYNATRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2004
Days to Decision
72 days
Submission Type
Summary