Last synced on 30 September 2022 at 11:05 pm

MODEL 150K LASER COAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832089
510(k) Type
Traditional
Applicant
LASERTEK OY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1984
Days to Decision
221 days

MODEL 150K LASER COAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K832089
510(k) Type
Traditional
Applicant
LASERTEK OY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1984
Days to Decision
221 days