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LENSX 550 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082947
510(k) Type
Traditional
Applicant
LENSX LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2009
Days to Decision
316 days
Submission Type
Summary

LENSX 550 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082947
510(k) Type
Traditional
Applicant
LENSX LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2009
Days to Decision
316 days
Submission Type
Summary