Last synced on 20 December 2024 at 11:05 pm

FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200022
510(k) Type
Traditional
Applicant
LiverMoreTech Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2020
Days to Decision
88 days
Submission Type
Summary

FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200022
510(k) Type
Traditional
Applicant
LiverMoreTech Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2020
Days to Decision
88 days
Submission Type
Summary