510(k) K192437

Device
Arterys MICA
Applicant
Arterys Inc.
510(k) number
K192437
Product code
QIH  
Decision
Substantially Equivalent (SESE)
Decision date
2020-03-25
Date received
2019-09-06
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Sharon Cholowsky
Address
51 Federal St., Suite 305 San Francisco CA US 94107 94107

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
B664AMM60Arterys MICAArterys Inc.2020-07-03

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Legacy Summary

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FDA Review

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