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EYECHEK

Page Type
Cleared 510(K)
510(k) Number
K964290
510(k) Type
Traditional
Applicant
Reichert Ophthalmic Instruments, Div. Leica, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1997
Days to Decision
73 days
Submission Type
Statement

EYECHEK

Page Type
Cleared 510(K)
510(k) Number
K964290
510(k) Type
Traditional
Applicant
Reichert Ophthalmic Instruments, Div. Leica, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1997
Days to Decision
73 days
Submission Type
Statement