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AUTO REF-KERATOMETER, RK-3

Page Type
Cleared 510(K)
510(k) Number
K942242
510(k) Type
Traditional
Applicant
CANNON U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1994
Days to Decision
116 days
Submission Type
Summary

AUTO REF-KERATOMETER, RK-3

Page Type
Cleared 510(K)
510(k) Number
K942242
510(k) Type
Traditional
Applicant
CANNON U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/1994
Days to Decision
116 days
Submission Type
Summary