Last synced on 25 April 2025 at 11:05 pm

SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082409
510(k) Type
Traditional
Applicant
ENDOPHOTONIX, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2009
Days to Decision
153 days
Submission Type
Summary

SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082409
510(k) Type
Traditional
Applicant
ENDOPHOTONIX, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2009
Days to Decision
153 days
Submission Type
Summary