Last synced on 30 May 2025 at 11:05 pm

KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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