Last synced on 4 February 2023 at 10:33 pm

MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895196
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1989
Days to Decision
66 days

MODEL DC-1200 DIODE LASER PHOTOCOAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895196
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1989
Days to Decision
66 days