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

Viz AAA

K Number: K223443 · Decision Mar 17, 2023
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
39
Applicant Total
11
Review Days
123

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Basic Information

Device Name
Viz AAA
K Number
K223443
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2080
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Viz. Ai, Inc.
Date Received
November 14, 2022
Decision Date
March 17, 2023
Product Code
QFM
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
QFM Radiological Computer-Assisted Prioritization Software For Lesions

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QFM), 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
K223042 Viz LVO ContaCT
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. →