EXONOX PERCUTANEOUS INTRODUCER SYSTEM W/ HEMOSTASI— 510(k) K923681

Substantially Equivalent

Exonix Research Corp.

FDA 510(k) clearance K923681 for EXONOX PERCUTANEOUS INTRODUCER SYSTEM W/ HEMOSTASI, Substantially Equivalent on 1993-01-21. Applicant: Exonix Research Corp..

Clearance details

Applicant: Exonix Research Corp.
Product code: Code DYB
Advisory panel: Cardiovascular
Date received: 1992-07-22
Decision date: 1993-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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Adverse events under product code DYB

product code DYB

Death: 808
Injury: 5,922
Malfunction: 16,516
Other: 5
Total: 23,251

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.