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LUXTEC ACO SERIES 4000 LIGHT SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890716
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1989
Days to Decision
72 days

LUXTEC ACO SERIES 4000 LIGHT SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890716
510(k) Type
Traditional
Applicant
LUXTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1989
Days to Decision
72 days