CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE— 510(k) K921147

Name: FDA 510(k) clearance K921147
Creator: U.S. Food and Drug Administration
Published: 1992-06-16

Substantially Equivalent

Cardiovascular Imaging Systems, Inc.

FDA 510(k) clearance K921147 for CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE, Substantially Equivalent on 1992-06-16. Applicant: Cardiovascular Imaging Systems, Inc.. Device class: 2.

Clearance details

Applicant: Cardiovascular Imaging Systems, Inc.
Product code: Code ITX
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 1992-03-11
Decision date: 1992-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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K942231 — MICROVIEW II/MICRORAIL II CATHETERS1994-08-01
K933517 — AUTOMATIC PULL BACK DEVICE1993-10-15
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Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.