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Ultrasonic Endo Activation Device (Model:Actor I pro)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213947
510(k) Type
Traditional
Applicant
ChangZhou BoMedent Medical Technology Co.,Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/8/2022
Days to Decision
265 days
Submission Type
Summary

Ultrasonic Endo Activation Device (Model:Actor I pro)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213947
510(k) Type
Traditional
Applicant
ChangZhou BoMedent Medical Technology Co.,Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/8/2022
Days to Decision
265 days
Submission Type
Summary