TRI-LUMEN INTRA VASCULAR BALLOON CATHETER— 510(k) K891021

Name: FDA 510(k) clearance K891021
Creator: U.S. Food and Drug Administration
Published: 1989-09-18

Substantially Equivalent

Ideal Medical, Inc.

FDA 510(k) clearance K891021 for TRI-LUMEN INTRA VASCULAR BALLOON CATHETER, Substantially Equivalent on 1989-09-18. Applicant: Ideal Medical, Inc.. Device class: 2.

Clearance details

Applicant: Ideal Medical, Inc.
Product code: Code DXE
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 1989-02-28
Decision date: 1989-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DXE

product code DXE

Death: 27
Injury: 258
Malfunction: 2,266
Total: 2,551

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.