CVD SMALL VESSEL BALLOON DILATION CATHETER— 510(k) K942150

Name: FDA 510(k) clearance K942150
Creator: U.S. Food and Drug Administration
Published: 1994-08-02

Substantially Equivalent

Cardio-Dynamics, Inc.

FDA 510(k) clearance K942150 for CVD SMALL VESSEL BALLOON DILATION CATHETER, Substantially Equivalent on 1994-08-02. Applicant: Cardio-Dynamics, Inc.. Device class: 2.

Clearance details

Applicant: Cardio-Dynamics, Inc.
Product code: Code LIT
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 1994-05-03
Decision date: 1994-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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K954313 — FOCUS PC BALLOON DILATATION CATHETER1995-12-01
K945943 — CVD PERIFLOW(TM) BALLOON DILATATION CATHETER1995-02-24
K931027 — BULLETT PERIPHERAL INFUSION CATHETER1994-02-04

Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

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.