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DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031329
510(k) Type
Traditional
Applicant
DYNATRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2003
Days to Decision
177 days
Submission Type
Summary

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031329
510(k) Type
Traditional
Applicant
DYNATRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2003
Days to Decision
177 days
Submission Type
Summary