ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETS— 510(k) K091593

Substantially Equivalent

Possis Medical, Inc.

FDA 510(k) clearance K091593 for ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETS, Substantially Equivalent on 2009-06-22. Applicant: Possis Medical, Inc..

Clearance details

Applicant: Possis Medical, Inc.
Product code: Code QEZ
Advisory panel: Cardiovascular
Date received: 2009-06-02
Decision date: 2009-06-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Minneapolis, MN, US

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Adverse events under product code QEZ

product code QEZ

Death: 24
Total: 24

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.