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RESUBMITTED DIODE LASER COAGULATOR

Page Type
Cleared 510(K)
510(k) Number
K882372
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1988
Days to Decision
68 days

RESUBMITTED DIODE LASER COAGULATOR

Page Type
Cleared 510(K)
510(k) Number
K882372
510(k) Type
Traditional
Applicant
COOPERVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1988
Days to Decision
68 days