Last synced on 9 May 2025 at 11:05 pm

Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220877
510(k) Type
Traditional
Applicant
Lumenis Be, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
112 days
Submission Type
Summary

Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220877
510(k) Type
Traditional
Applicant
Lumenis Be, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
112 days
Submission Type
Summary