Last synced on 20 December 2024 at 11:05 pm

THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091783
510(k) Type
Special
Applicant
AVANTIS MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2009
Days to Decision
20 days
Submission Type
Summary

THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091783
510(k) Type
Special
Applicant
AVANTIS MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/2009
Days to Decision
20 days
Submission Type
Summary