Last synced on 25 April 2025 at 11:05 pm

COHERENT XA-50, X30/CW, XA30/SP SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895143
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1989
Days to Decision
38 days

COHERENT XA-50, X30/CW, XA30/SP SURGICAL LASERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895143
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1989
Days to Decision
38 days