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Smart Laser Indirect Ophthalmoscope (LIO); Laser delivery device for Lumenis Novus Spectra Laser System, Lumenis Vision One Laser System, and Lumenis Smart532™ Laser System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162837
510(k) Type
Traditional
Applicant
Lumenis, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/28/2017
Days to Decision
140 days
Submission Type
Summary

Smart Laser Indirect Ophthalmoscope (LIO); Laser delivery device for Lumenis Novus Spectra Laser System, Lumenis Vision One Laser System, and Lumenis Smart532™ Laser System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162837
510(k) Type
Traditional
Applicant
Lumenis, Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/28/2017
Days to Decision
140 days
Submission Type
Summary