Last synced on 14 November 2025 at 11:06 pm

COAGULATOR, MODEL 40 AARGON

Page Type
Cleared 510(K)
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)
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