SelectFlex 072 Neurovascular Access System— 510(k) K181000

Substantially Equivalent

Q'Apel

FDA 510(k) clearance K181000 for SelectFlex 072 Neurovascular Access System, Substantially Equivalent on 2018-09-13. Applicant: Q'Apel.

Clearance details

Applicant: Q'Apel
Product code: Code DQY
Advisory panel: Cardiovascular
Date received: 2018-04-16
Decision date: 2018-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, CA, US

Download summary PDF View on FDA.gov ↗

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.