Last synced on 14 November 2025 at 11:06 pm

VANTAGE INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K060822
510(k) Type
Special
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2006
Days to Decision
57 days
Submission Type
Summary

VANTAGE INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K060822
510(k) Type
Special
Applicant
KEELER INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2006
Days to Decision
57 days
Submission Type
Summary