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

GEMSS Medical System Surgical Mobile Fluoroscopic X-ray System

K Number: K160065 · Decision May 20, 2016
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
81
Applicant Total
4
Review Days
128

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Basic Information

Device Name
GEMSS Medical System Surgical Mobile Fluoroscopic X-ray System
K Number
K160065
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gemss Medical Systems Co., Ltd.
Date Received
January 13, 2016
Decision Date
May 20, 2016
Product Code
OXO
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
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

Similar 510(k) Clearances

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

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Other Clearances by Gemss Medical Systems Co., Ltd.

K Number Device Name
K163140 SPINEL 12HD Interventional Fluoroscopic Mobile X-ray System
K133695 TITAN 11
K132289 GEMSS MEDICAL SYSTEMS SURGICAL MOBILE FLUOROSCOPIC X-RAY SYSTEM