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LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032991
510(k) Type
Traditional
Applicant
LIGHT AGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2004
Days to Decision
355 days
Submission Type
Summary

LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032991
510(k) Type
Traditional
Applicant
LIGHT AGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2004
Days to Decision
355 days
Submission Type
Summary