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VISTA SPECIALIST OPHTHALMOSCOPE (BATTERY & AC)

Page Type
Cleared 510(K)
510(k) Number
K893173
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1989
Days to Decision
41 days

VISTA SPECIALIST OPHTHALMOSCOPE (BATTERY & AC)

Page Type
Cleared 510(K)
510(k) Number
K893173
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1989
Days to Decision
41 days