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

GEMSS MEDICAL SYSTEMS SURGICAL MOBILE FLUOROSCOPIC X-RAY SYSTEM

K Number: K132289 · Decision Jun 16, 2014
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
4
Review Days
328

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Basic Information

Device Name
GEMSS MEDICAL SYSTEMS SURGICAL MOBILE FLUOROSCOPIC X-RAY SYSTEM
K Number
K132289
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
July 23, 2013
Decision Date
June 16, 2014
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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Other 510(k) clearances with the same product code (JAA), 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
K160065 GEMSS Medical System Surgical Mobile Fluoroscopic X-ray System
K133695 TITAN 11