Last synced on 25 January 2026 at 3:41 am

EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VIDAPORT INTRAOSSEOUS INFUSION SYSTEM, EZ-IO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091140
510(k) Type
Traditional
Applicant
Vidacare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2009
Days to Decision
177 days
Submission Type
Summary

EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VIDAPORT INTRAOSSEOUS INFUSION SYSTEM, EZ-IO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091140
510(k) Type
Traditional
Applicant
Vidacare Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2009
Days to Decision
177 days
Submission Type
Summary