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CORNEASCOPE MODEL 1200

Page Type
Cleared 510(K)
510(k) Number
K850665
510(k) Type
Traditional
Applicant
KERA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1985
Days to Decision
28 days

CORNEASCOPE MODEL 1200

Page Type
Cleared 510(K)
510(k) Number
K850665
510(k) Type
Traditional
Applicant
KERA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1985
Days to Decision
28 days