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

DIGITAL X-RAY IMAGING SYSTEM, MODEL DRC-1000

K Number: K092830 · Decision Jul 21, 2010
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
40
Review Days
310

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Basic Information

Device Name
DIGITAL X-RAY IMAGING SYSTEM, MODEL DRC-1000
K Number
K092830
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VATECH Co., Ltd.
Date Received
September 14, 2009
Decision Date
July 21, 2010
Product Code
KPR
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
KPR System, X-Ray, Stationary

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K231796 Grreen X 12 (Model: PHT-75CHS)
K223058 EzRay Air 2 Wall (Model: VEX-S350W)
K213462 EzRay M18 (Model: VMX-P400)
K210329 Green X 18(Model : PHT-75CHS)
K203667 EzRay M (Model: VMX-P300)
K203797 vatech A9 (Model : PHT-30CSS)
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