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RESUBMITTED DIODE LASER COAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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