ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE— 510(k) K122690

Substantially Equivalent

Arrow International, Inc.

FDA 510(k) clearance K122690 for ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE, Substantially Equivalent on 2012-12-21. Applicant: Arrow International, Inc..

Clearance details

Applicant: Arrow International, Inc.
Product code: Code CAZ
Advisory panel: Anesthesiology
Date received: 2012-09-04
Decision date: 2012-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Reading, PA, US

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Adverse events under product code CAZ

product code CAZ

Injury: 145
Malfunction: 942
Other: 1
Total: 1,088

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.