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COAGULATOR, MODEL 40 AARGON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K782106
510(k) Type
Traditional
Applicant
LASERTEK OY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1979
Days to Decision
57 days

COAGULATOR, MODEL 40 AARGON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K782106
510(k) Type
Traditional
Applicant
LASERTEK OY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1979
Days to Decision
57 days