510(k) K231986

Device
Modus IR
Applicant
Synaptive Medical, Inc.
510(k) number
K231986
Product code
IZI
Decision
Substantially Equivalent (SESE)
Decision date
2024-03-25
Date received
2023-07-05
Regulation
892.1600
Classification name
System, X-Ray, Angiographic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Tahmina Afzali
Address
555 Richmond St. W., Suite 800 Toronto CA M5V 3B1 M5V 3B1

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
00670082000603Modus IRSynaptive Medical Inc2024-04-02

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