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PALOMAR DERMALUX PULSED LIGHT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010618
510(k) Type
Traditional
Applicant
PALOMAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/2001
Days to Decision
193 days
Submission Type
Summary

PALOMAR DERMALUX PULSED LIGHT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010618
510(k) Type
Traditional
Applicant
PALOMAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/2001
Days to Decision
193 days
Submission Type
Summary