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Diode Laser Hair Removal Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221312
510(k) Type
Traditional
Applicant
Guangzhou CHUANG ZAO MEI Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/29/2022
Days to Decision
55 days
Submission Type
Summary

Diode Laser Hair Removal Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221312
510(k) Type
Traditional
Applicant
Guangzhou CHUANG ZAO MEI Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/29/2022
Days to Decision
55 days
Submission Type
Summary