Last synced on 2 June 2023 at 11:04 pm

LUXTEC MLX LIGHT SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081477
510(k) Type
Traditional
Applicant
INTEGRA LUXTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2008
Days to Decision
22 days
Submission Type
Statement

LUXTEC MLX LIGHT SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081477
510(k) Type
Traditional
Applicant
INTEGRA LUXTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2008
Days to Decision
22 days
Submission Type
Statement