MedAI Verdict
Radiology

AI Radiology

MaxQ AI Accipio

by MaxQ AI  ·  IL

Last verified

Accipio flagged suspected intracranial haemorrhage on head CT. MaxQ AI stopped operations in January 2022 and discontinued it.

At a glance

Pricing
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HIPAA
Not disclosed
SOC 2
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EHRs
—
Founded
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HQ
IL
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Bottom line

Accipio flagged suspected intracranial haemorrhage on head CT. MaxQ AI stopped operations in January 2022 and discontinued it.

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Editorial review  ·  By MedAI Verdict

Bottom line

Accipio was an AI tool from the Israeli company MaxQ AI that flagged suspected intracranial haemorrhage on non-contrast head CT and moved those scans up the worklist. The Imaging Wire reported in January 2022 that MaxQ AI stopped commercial operations, and AuntMinnie reported that the company was discontinuing Accipio and ending its image-analysis AI work.

What was Accipio?

AuntMinnie describes Accipio as software for detecting and triaging intracranial haemorrhage, also called ICH, on head CT. MaxQ later launched a second-generation Accipio clinical platform, announced through PRWeb. Versions called Accipio Ix and Ax were offered on the Nuance AI Marketplace, and the product was also distributed through the Blackford platform from December 2019.

What did the FDA clear?

The FDA's 510(k) records list two clearances for the product under the applicant name Maxq-Al, Ltd., both for the device listed as Accipiolx in product code QAS:

  • K182177, October 2018
  • K201310, August 2020

What happened to the company?

The Imaging Wire framed the January 2022 shutdown, which came with layoffs of sales and marketing staff, as an opening for competing ICH products, and named Qure.ai, Aidoc and Avicenna.ai as rivals that benefited. It also reported that neither Qure.ai nor Nuance acquired MaxQ.

The verdict

Accipio was cleared in October 2018 and again in August 2020, and was discontinued in early 2022.

Editorial review last generated October 15, 2026. Synthesized from clinician sentiment, peer-reviewed coverage, and our editorial silo picks. Refined by hand where vendor facts change.

Compliance + integration

What deploys cleanly

Carries FDA 510(k) per vendor documentation. Independent attestation review is the buyer's responsibility before clinical deployment.