Last synced on 30 September 2022 at 11:05 pm

NIDEK KM-800 AUTO KERATOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861063
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1986
Days to Decision
15 days

NIDEK KM-800 AUTO KERATOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861063
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1986
Days to Decision
15 days