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MODEL 2000 INTRAOPERATIVE CORNEASCOPE

Page Type
Cleared 510(K)
510(k) Number
K901009
510(k) Type
Traditional
Applicant
KERA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1990
Days to Decision
86 days

MODEL 2000 INTRAOPERATIVE CORNEASCOPE

Page Type
Cleared 510(K)
510(k) Number
K901009
510(k) Type
Traditional
Applicant
KERA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1990
Days to Decision
86 days