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NIDEK KM-800 AUTO KERATOMETER

Page Type
Cleared 510(K)
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)
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