Ischemaview, Inc.
Ischemaview, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2025.
Top product codes for Ischemaview, Inc.
Recent clearances by Ischemaview, Inc.
- K251987 — Rapid Aortic Measurements
- K251533 — Rapid Obstructive Hydrocephalus, Rapid OH
- K252526 — Rapid DeltaFuse
- K243378 — Rapid MLS
- K243350 — Rapid Neuro3D
- K233582 — Rapid
- K232156 — Rapid ASPECTS (v3)
- K233512 — Rapid (6.0)
- K232436 — Rapid SDH
- K230074 — Rapid Aneurysm Triage and Notification
- K222884 — Rapid NCCT Stroke
- K223396 — Rapid RV/LV
- K221456 — Rapid ICH
- K221248 — Rapid LVO
- K220499 — Rapid PE Triage and Notification (PETN)
- K213165 — Rapid
- K200941 — Rapid LVO
- K200760 — Rapid ASPECTS
- K182130 — iSchemaView RAPID
- K172477 — iSchemaView RAPID
- K121447 — ISCHEMA VIEW RAPID
Data sourced from openFDA. This site is unofficial and independent of the FDA.