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KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004

Page Type
Cleared 510(K)
510(k) Number
K032087
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2003
Days to Decision
142 days
Submission Type
Summary

KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004

Page Type
Cleared 510(K)
510(k) Number
K032087
510(k) Type
Traditional
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2003
Days to Decision
142 days
Submission Type
Summary