DESERET EMBOLECTOMY/THROMBECTOMY CATH.— 510(k) K801650

Name: FDA 510(k) clearance K801650
Creator: U.S. Food and Drug Administration
Published: 1980-08-04

Substantially Equivalent

Deseret Medical, Inc.

FDA 510(k) clearance K801650 for DESERET EMBOLECTOMY/THROMBECTOMY CATH., Substantially Equivalent on 1980-08-04. Applicant: Deseret Medical, Inc.. Device class: 2.

Clearance details

Applicant: Deseret Medical, Inc.
Product code: Code DXE
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 1980-07-18
Decision date: 1980-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.