FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

PRECISION RXI ANALOG X-RAY SYSTEM

K Number: K041605 · Decision Jun 30, 2004
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
7
Review Days
15

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Basic Information

Device Name
PRECISION RXI ANALOG X-RAY SYSTEM
K Number
K041605
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
General Medical Merate S.P.A
Date Received
June 15, 2004
Decision Date
June 30, 2004
Product Code
OWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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

Other 510(k) clearances with the same product code (OWB), ordered by most recent decision date.

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Other Clearances by General Medical Merate S.P.A

K Number Device Name
K213081 CLISIS SYSTEMS, Discovery RF180
K173395 MECALL CLISIS SYSTEMS, Discovery RF180
K140380 OPERA SWING
K082243 PRECISION RXI ANALOG AND DIGITAL X-RAY SYSTEMS
K881386 X-RAY GENERATING SYSTEM TF 1000
K827993 MTH C/A MOBILE C ARM