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THE KEELER ALL PUPIL INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K854244
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1985
Days to Decision
22 days

THE KEELER ALL PUPIL INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K854244
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1985
Days to Decision
22 days