SUBMARINE PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SUVXXXXXXXXX— 510(k) K042537

Name: FDA 510(k) clearance K042537
Creator: U.S. Food and Drug Administration
Published: 2004-11-08

Substantially Equivalent

Invatec Innovative Technologies

FDA 510(k) clearance K042537 for SUBMARINE PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SUVXXXXXXXXX, Substantially Equivalent on 2004-11-08. Applicant: Invatec Innovative Technologies. Device class: 2.

Clearance details

Applicant: Invatec Innovative Technologies
Product code: Code DQY
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 2004-09-20
Decision date: 2004-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plymouth, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DQY

product code DQY

Death: 464
Injury: 4,489
Malfunction: 13,721
Other: 2
Total: 18,676

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.