CAVITRON ULTRASONIC SURG. ASPIR. CUSA— 510(k) K801623

Substantially Equivalent

Cavitron Corp.

FDA 510(k) clearance K801623 for CAVITRON ULTRASONIC SURG. ASPIR. CUSA, Substantially Equivalent on 1980-11-18. Applicant: Cavitron Corp..

Clearance details

Applicant: Cavitron Corp.
Product code: Code LFL
Advisory panel: Unknown
Date received: 1980-07-15
Decision date: 1980-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code LFL

product code LFL

Death: 29
Injury: 1,046
Malfunction: 21,642
Total: 22,717

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.