510(k) K232779

Device
QUEX ED; QUEX S
Applicant
Qx World, Ltd.
510(k) number
K232779
Product code
OMC
Decision
Substantially Equivalent (SESE)
Decision date
2024-10-11
Date received
2023-09-11
Regulation
882.1400
Classification name
Reduced- Montage Standard Electroencephalograph
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Lilla Strobel
Address
Tinodi Utca 1-3 A.Ep, Iv.Em, 93 Budapest HU 1095 1095

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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