MISONIX INC. FS 1000 RF ULTRASONIC SURGICAL ASPIRATOR SYSTEM— 510(k) K032690

Name: FDA 510(k) clearance K032690
Creator: U.S. Food and Drug Administration
Published: 2003-12-09

Substantially Equivalent

Misonix, Inc.

FDA 510(k) clearance K032690 for MISONIX INC. FS 1000 RF ULTRASONIC SURGICAL ASPIRATOR SYSTEM, Substantially Equivalent on 2003-12-09. Applicant: Misonix, Inc.. Device class: Unclassified.

Clearance details

Applicant: Misonix, Inc.
Product code: Code LFL
Device class: Unclassified
Advisory panel: Unknown
Date received: 2003-09-02
Decision date: 2003-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

Download summary PDF View on FDA.gov ↗

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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.