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LASER, PHOTOCOAGULATION

Page Type
Cleared 510(K)
510(k) Number
K782065
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1978
Days to Decision
15 days

LASER, PHOTOCOAGULATION

Page Type
Cleared 510(K)
510(k) Number
K782065
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/1978
Days to Decision
15 days