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OMNILIGHT FLUORESCENT PULSED LIGHT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032191
510(k) Type
Special
Applicant
LUXSANO AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2003
Days to Decision
34 days
Submission Type
Summary

OMNILIGHT FLUORESCENT PULSED LIGHT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032191
510(k) Type
Special
Applicant
LUXSANO AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2003
Days to Decision
34 days
Submission Type
Summary