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NIDEK MODEL AKC-8000 OPHTHALMIC LASER PHOTOCOAGULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900890
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1990
Days to Decision
195 days

NIDEK MODEL AKC-8000 OPHTHALMIC LASER PHOTOCOAGULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900890
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1990
Days to Decision
195 days