FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

GXR-ES/ECS Diagnostic X-Ray System, (Models GXR-ES series, GXR-ECS series)

K Number: K232178 · Decision Sep 19, 2023
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
14
Review Days
57

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Basic Information

Device Name
GXR-ES/ECS Diagnostic X-Ray System, (Models GXR-ES series, GXR-ECS series)
K Number
K232178
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
July 24, 2023
Decision Date
September 19, 2023
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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Other Clearances by DRGEM Corporation

K Number Device Name
K260085 RAYMO Mobile X-ray System (Model: RAYMO)
K251443 PROMO
K242019 GXR-Series Diagnostic X-Ray System
K242015 TOPAZ Mobile X-ray System (Models : TOPAZ-32D, TOPAZ-40D)
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
K183292 Topaz Mobile DR System
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