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Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241057
510(k) Type
Traditional
Applicant
Wuhan Guangdun Technology Co.,Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/24/2025
Days to Decision
281 days
Submission Type
Summary

Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241057
510(k) Type
Traditional
Applicant
Wuhan Guangdun Technology Co.,Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/24/2025
Days to Decision
281 days
Submission Type
Summary