Rapid— 510(k) K213165

Substantially Equivalent

Ischemaview, Inc.

FDA 510(k) clearance K213165 for Rapid, Substantially Equivalent on 2022-02-08. Applicant: Ischemaview, Inc..

Clearance details

Applicant: Ischemaview, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2021-09-28
Decision date: 2022-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Golden, CO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.