MISONIX INC. LYSONIX 2000/3000 ULTRASONIC SURGICAL ASPIRATOR SYSTEMS— 510(k) K041058

Name: FDA 510(k) clearance K041058
Creator: U.S. Food and Drug Administration
Published: 2004-05-17

Substantially Equivalent

Misonix, Inc.

FDA 510(k) clearance K041058 for MISONIX INC. LYSONIX 2000/3000 ULTRASONIC SURGICAL ASPIRATOR SYSTEMS, Substantially Equivalent on 2004-05-17. Applicant: Misonix, Inc.. Device class: 2.

Clearance details

Applicant: Misonix, Inc.
Product code: Code QPB
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2004-04-23
Decision date: 2004-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

Download summary PDF View on FDA.gov ↗

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