QScreen

Stimulator, Auditory, Evoked Response

PATH MEDICAL GmbH

The following data is part of a premarket notification filed by Path Medical Gmbh with the FDA for Qscreen.

Pre-market Notification Details

Device IDK220139
510k NumberK220139
Device Name:QScreen
ClassificationStimulator, Auditory, Evoked Response
Applicant PATH MEDICAL GmbH Landsberger Strasse 65 Germering,  DE 82110
ContactJohann Oswald
CorrespondentJohann Oswald
PATH MEDICAL GmbH Landsberger Strasse 65 Germering,  DE 82110
Product CodeGWJ  
CFR Regulation Number882.1900 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2022-01-18
Decision Date2022-08-03

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
04260223145889 K220139 000
04260223146336 K220139 000
04260223146329 K220139 000
04260223146312 K220139 000
04260223146305 K220139 000
04260223146299 K220139 000
04260223146282 K220139 000
04260223146275 K220139 000
04260223146268 K220139 000
04260223146343 K220139 000
04260223146534 K220139 000
04260223146541 K220139 000
04260223145766 K220139 000
04260223146725 K220139 000
04260223146688 K220139 000
04260223146671 K220139 000
04260223146664 K220139 000
04260223146657 K220139 000
04260223146565 K220139 000
04260223146558 K220139 000
04260223146251 K220139 000

Trademark Results [QScreen]

Mark Image

Registration | Serial
Company
Trademark
Application Date
QSCREEN
QSCREEN
88019765 not registered Dead/Abandoned
International Health Options Inc.
2018-06-28
QSCREEN
QSCREEN
87006492 5312496 Live/Registered
Quest Diagnostics Investments LLC
2016-04-19
QSCREEN
QSCREEN
79254894 5847878 Live/Registered
Barnes Group Suisse Industries GmbH
2019-02-21

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