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

DIGITAL DIAGNOSTIC X-RAY SYSTEM

K Number: K102408 · Decision Dec 27, 2010
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
14
Review Days
126

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Basic Information

Device Name
DIGITAL DIAGNOSTIC X-RAY SYSTEM
K Number
K102408
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DRGEM Corporation
Date Received
August 23, 2010
Decision Date
December 27, 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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K Number Device Name
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K251443 PROMO
K242019 GXR-Series Diagnostic X-Ray System
K242015 TOPAZ Mobile X-ray System (Models : TOPAZ-32D, TOPAZ-40D)
K232178 GXR-ES/ECS Diagnostic X-Ray System, (Models GXR-ES series, GXR-ECS series)
K202572 GXR-Series Diagnostic X-Ray System
K202156 DIAMOND-5A/6A/8A
K201124 TOPAZ Mobile DR System
K192453 DIAMOND-5A/6A/8A
K192364 GXR-Series Diagnostic X-Ray System
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