FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

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

K Number: K200022 · Decision Apr 3, 2020
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
6
Review Days
88

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Basic Information

Device Name
FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System
K Number
K200022
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Livermoretech, Inc.
Date Received
January 6, 2020
Decision Date
April 3, 2020
Product Code
OWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OWB Interventional Fluoroscopic X-Ray System

Similar 510(k) Clearances

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K193644 E-COM DR-2000 DR
K190935 EZER, Portable X-ray System
K180663 LaVid FMTS DIAGNOSTIC X-RAY SYSTEM