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LASEREX DUO FAMILY OF DUAL WAVELENGTH OPHTHALMIC LASERS INCLUDING MODELS INTEGRE DUO LP1RG-S, LP1RG-D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052777
510(k) Type
Traditional
Applicant
Ellex Medical Pty. Ltd.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
3/16/2006
Days to Decision
164 days
Submission Type
Statement

LASEREX DUO FAMILY OF DUAL WAVELENGTH OPHTHALMIC LASERS INCLUDING MODELS INTEGRE DUO LP1RG-S, LP1RG-D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052777
510(k) Type
Traditional
Applicant
Ellex Medical Pty. Ltd.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
3/16/2006
Days to Decision
164 days
Submission Type
Statement