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LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072048
510(k) Type
Traditional
Applicant
LYNTON LASERS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/16/2007
Days to Decision
114 days
Submission Type
Summary

LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072048
510(k) Type
Traditional
Applicant
LYNTON LASERS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/16/2007
Days to Decision
114 days
Submission Type
Summary