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AUTOKERATOMETER, INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K781994
510(k) Type
Traditional
Applicant
ZEISS HUMPHREY SYSTEM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1979
Days to Decision
75 days

AUTOKERATOMETER, INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K781994
510(k) Type
Traditional
Applicant
ZEISS HUMPHREY SYSTEM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1979
Days to Decision
75 days