Last synced on 30 September 2022 at 11:05 pm

27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110951
510(k) Type
Traditional
Applicant
ALCON RESEARCH, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2011
Days to Decision
196 days
Submission Type
Summary

27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110951
510(k) Type
Traditional
Applicant
ALCON RESEARCH, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2011
Days to Decision
196 days
Submission Type
Summary