Last synced on 22 September 2023 at 11:04 pm

ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862456
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1986
Days to Decision
46 days

ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862456
510(k) Type
Traditional
Applicant
COOPER LASERSONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1986
Days to Decision
46 days