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XPERT NCT

Page Type
Cleared 510(K)
510(k) Number
K941865
510(k) Type
Traditional
Applicant
REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1994
Days to Decision
164 days
Submission Type
Statement

XPERT NCT

Page Type
Cleared 510(K)
510(k) Number
K941865
510(k) Type
Traditional
Applicant
REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1994
Days to Decision
164 days
Submission Type
Statement