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

EzRay M18 (Model: VMX-P400)

K Number: K213462 · Decision Feb 11, 2022
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
40
Review Days
107

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EzRay M18 (Model: VMX-P400)
K Number
K213462
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VATECH Co., Ltd.
Date Received
October 27, 2021
Decision Date
February 11, 2022
Product Code
IZL
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
IZL System, X-Ray, Mobile

Similar 510(k) Clearances

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

View all

Other Clearances by VATECH Co., Ltd.

K Number Device Name
K260093 Green X 12 VE (PHT-70CHS); Green X VE (PHT-70CHS)
K243088 Green X 12 SE (PHT-40CHS)
K243081 Green X 21 (PHT-90CHO)
K240040 VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)
K231796 Grreen X 12 (Model: PHT-75CHS)
K223058 EzRay Air 2 Wall (Model: VEX-S350W)
K210329 Green X 18(Model : PHT-75CHS)
K203667 EzRay M (Model: VMX-P300)
K203797 vatech A9 (Model : PHT-30CSS)
K201627 Dental Computed Tomography X-Ray System, Green X
Search all 40 clearances from VATECH Co., Ltd. →