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SOLX 790 TITANIUM SAPPHIRE LASER

Page Type
Cleared 510(K)
510(k) Number
K081774
510(k) Type
Traditional
Applicant
SOLX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
81 days
Submission Type
Summary

SOLX 790 TITANIUM SAPPHIRE LASER

Page Type
Cleared 510(K)
510(k) Number
K081774
510(k) Type
Traditional
Applicant
SOLX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
81 days
Submission Type
Summary