Medical Device Manufacturer · US , Irvine , CA

Ischemaview, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2013

Total

Cleared

Denied

Ischemaview, Inc. has 21 FDA 510(k) cleared radiology devices. Based in Irvine, US.

Latest FDA clearance: Sep 2025. Active since 2013.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ischemaview, Inc.

21 devices

1-21 of 21

Cleared Sep 23, 2025

Rapid Aortic Measurements

K251987 · QIH

Radiology · 88d

Cleared Sep 04, 2025

Rapid Obstructive Hydrocephalus, Rapid OH

Rapid Aneurysm Triage and Notification

Rapid PE Triage and Notification (PETN)

Ischemaview, Inc. - FDA 510(k) Cleared Devices

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