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KEELER VANTAGE INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K942104
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1994
Days to Decision
94 days
Submission Type
Statement

KEELER VANTAGE INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K942104
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1994
Days to Decision
94 days
Submission Type
Statement