Last synced on 23 September 2022 at 11:05 pm

DC-3300 LASER DIODE PHOTOCOAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013760
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2002
Days to Decision
90 days
Submission Type
Summary

DC-3300 LASER DIODE PHOTOCOAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013760
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2002
Days to Decision
90 days
Submission Type
Summary