neXus Ultrasonic Surgical Aspirator System
K-Number: K190160 · 2019-05-30
Device Summary
Frequently Asked Questions
What is the neXus Ultrasonic Surgical Aspirator System?
neXus Ultrasonic Surgical Aspirator System is a medical device that received FDA 510(k) clearance on 2019-05-30. The listed applicant is Misonix, Inc.. The 510(k) number is K190160.
When did neXus Ultrasonic Surgical Aspirator System receive FDA 510(k) clearance?
neXus Ultrasonic Surgical Aspirator System received FDA 510(k) clearance on 2019-05-30, under 510(k) number K190160.
Who is the listed applicant for neXus Ultrasonic Surgical Aspirator System?
The FDA 510(k) record lists Misonix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for neXus Ultrasonic Surgical Aspirator System?
The FDA product code for neXus Ultrasonic Surgical Aspirator System is LFL.
Other records listing Misonix, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LFL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.