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MODEL 150K LASER COAGULATOR

Page Type
Cleared 510(K)
PDF
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
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