Last synced on 25 April 2025 at 11:05 pm

LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063427
510(k) Type
Traditional
Applicant
LYNTON LASERS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/25/2007
Days to Decision
254 days
Submission Type
Summary

LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063427
510(k) Type
Traditional
Applicant
LYNTON LASERS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/25/2007
Days to Decision
254 days
Submission Type
Summary