FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

CAAS Workstation

K Number: K232147 · Decision Apr 9, 2024
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
6
Applicant Total
23
Review Days
265

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Basic Information

Device Name
CAAS Workstation
K Number
K232147
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pie Medical Imaging BV
Date Received
July 19, 2023
Decision Date
April 9, 2024
Product Code
QHA
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
QHA X-Ray Angiographic Imaging Based Coronary Vascular Simulation Software Device

Similar 510(k) Clearances

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

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Other Clearances by Pie Medical Imaging BV

K Number Device Name
K250330 3mensio Workstation
K232007 CAAS MR Solutions
K212376 Caas Qardia
K181825 CAAS MR Solutions
K180019 CAAS Workstation
K162376 CAAS MR 4D Flow
K162112 CAAS MRV
K153736 3mensio Workstation
K151780 CAAS Workstation
K143044 CAAS A-Valve
Search all 23 clearances from Pie Medical Imaging BV →