FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

QScreen

K Number: K220139 · Decision Aug 3, 2022
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
6
Review Days
197

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
QScreen
K Number
K220139
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1900
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Path Medical GmbH
Date Received
January 18, 2022
Decision Date
August 3, 2022
Product Code
GWJ
Advisory Committee
Neurology
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWJ Stimulator, Auditory, Evoked Response

Similar 510(k) Clearances

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

View all

Other Clearances by Path Medical GmbH

K Number Device Name
K213345 Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONE
K211147 ALGO 7i
K133012 SENTIERO
K131141 EARPROBE
K100661 EARPROBE