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AESCULIGHT FAMILY OF FLEXIBLE FIBERS, HANDPIECES AND TIPS FOR CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081612
510(k) Type
Traditional
Applicant
AESCULIGHT, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2008
Days to Decision
16 days
Submission Type
Summary

AESCULIGHT FAMILY OF FLEXIBLE FIBERS, HANDPIECES AND TIPS FOR CO2 SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081612
510(k) Type
Traditional
Applicant
AESCULIGHT, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2008
Days to Decision
16 days
Submission Type
Summary