GUIDEWIRE, PURSUER SERIES— 510(k) K130104

Substantially Equivalent

Oscor, Inc.

FDA 510(k) clearance K130104 for GUIDEWIRE, PURSUER SERIES, Substantially Equivalent on 2013-06-13. Applicant: Oscor, Inc..

Clearance details

Applicant: Oscor, Inc.
Product code: Code DQX
Advisory panel: Cardiovascular
Date received: 2013-01-15
Decision date: 2013-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Harbor, FL, US

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Adverse events under product code DQX

product code DQX

Death: 298
Injury: 4,385
Malfunction: 7,203
Other: 5
Total: 11,891

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.