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SOLX 790 TITANIUM SAPPHIRE LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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