Last synced on 14 November 2025 at 11:06 pm

NAVIX ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093279
510(k) Type
Traditional
Applicant
XLUMENA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2010
Days to Decision
169 days
Submission Type
Summary

NAVIX ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K093279
510(k) Type
Traditional
Applicant
XLUMENA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2010
Days to Decision
169 days
Submission Type
Summary