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

Viz LVO ContaCT

K Number: K223042 · Decision Oct 21, 2022
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
85
Applicant Total
11
Review Days
22

Basic Information

Device Name
Viz LVO ContaCT
K Number
K223042
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2080
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Viz. Ai, Inc.
Date Received
September 29, 2022
Decision Date
October 21, 2022
Product Code
QAS
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
QAS Radiological Computer-Assisted Triage And Notification Software

Similar 510(k) Clearances

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

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Other Clearances by Viz. Ai, Inc.

K Number Device Name
K250354 Viz Subdural+, Viz SUBDURAL PLUS
K232363 Viz HDS, Viz Volume Plus, Viz ICH+
DEN230003 Viz HCM
K223443 Viz AAA
K221100 Viz RV/LV
K220439 Viz SDH
K213319 Viz ANEURYSM, Viz ANX
K210209 Viz ICH
K193658 Viz ICH
K180161 Viz CTP
Search all 11 clearances from Viz. Ai, Inc. →