Last synced on 6 June 2025 at 11:06 pm

OPTIMEDICA LASER INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062336
510(k) Type
Traditional
Applicant
OPTIMEDICA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2006
Days to Decision
70 days
Submission Type
Summary

OPTIMEDICA LASER INDIRECT OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062336
510(k) Type
Traditional
Applicant
OPTIMEDICA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2006
Days to Decision
70 days
Submission Type
Summary