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FDA 510(k)

Rapid Vessel Occlusion (Rapid VO)

K-Number: K261085 · 2026-07-13

ApplicantiSchemaview
Decision Date2026-07-13
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Rapid Vessel Occlusion (Rapid VO) is the device name listed in this FDA 510(k) record. The listed applicant is iSchemaview. It received FDA 510(k) clearance on 2026-07-13 under 510(k) number K261085. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Rapid Vessel Occlusion (Rapid VO)?

Rapid Vessel Occlusion (Rapid VO) is a medical device that received FDA 510(k) clearance on 2026-07-13. The listed applicant is iSchemaview. The 510(k) number is K261085.

When did Rapid Vessel Occlusion (Rapid VO) receive FDA 510(k) clearance?

Rapid Vessel Occlusion (Rapid VO) received FDA 510(k) clearance on 2026-07-13, under 510(k) number K261085.

Who is the listed applicant for Rapid Vessel Occlusion (Rapid VO)?

The FDA 510(k) record lists iSchemaview as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Rapid Vessel Occlusion (Rapid VO)?

The FDA product code for Rapid Vessel Occlusion (Rapid VO) is QAS.

Other records listing iSchemaview as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251987Rapid Aortic MeasurementsK251533Rapid Obstructive Hydrocephalus, Rapid OHK252526Rapid DeltaFuseK251151Rapid CTA 360K243378Rapid MLSK243350Rapid Neuro3D

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Related Devices (Code: QAS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260729Vascular Assist Occlusion Triage (VAOT) (v1.0)GuideAI HealthK261317BriefCase-TriageAidoc Medical , Ltd.K253163EFAI ERSUITE CT APPENDICITIS ASSESSMENT SYSTEM (APPEN-CT-100)Ever Fortune.Ai, Co., Ltd.K252421JLK-NCCTJLK, Inc.K253818Annalise EnterpriseHarrison-AI Medical Pty, Ltd.K253578BriefCase-Triage: CARE Multi-Triage CT for Pneumothorax; Pericardial effusion; Large aortic aneurysm; Shoulder fracture or dislocation deviceAidoc Medical , Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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