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Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181121
510(k) Type
Traditional
Applicant
Home Well Trading LTD
Country
British Virgin Islands
FDA Decision
Substantially Equivalent
Decision Date
6/28/2018
Days to Decision
59 days
Submission Type
Summary

Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181121
510(k) Type
Traditional
Applicant
Home Well Trading LTD
Country
British Virgin Islands
FDA Decision
Substantially Equivalent
Decision Date
6/28/2018
Days to Decision
59 days
Submission Type
Summary