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NIDEK AC-2000 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K860011
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
35 days

NIDEK AC-2000 LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K860011
510(k) Type
Traditional
Applicant
NIDEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
35 days