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

DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16

K Number: K080553 · Decision Apr 16, 2008
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
21
Review Days
48

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Basic Information

Device Name
DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16
K Number
K080553
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vieworks Co., Ltd.
Date Received
February 28, 2008
Decision Date
April 16, 2008
Product Code
KPR
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
KPR System, X-Ray, Stationary

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K241113 VIVIX-M
K241125 VIVIX-S 1751S
K220239 Solid State X-ray Imager(Model: FXRD-4386WB)
K221512 Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW)
K200418 VIVIX-S VW
K190611 VIVIX-S 1751S
K181003 VIVIX-S 1717V
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