510(k) K190160

neXus Ultrasonic Surgical Aspirator System by Misonix, Inc. — Product Code LFL

K190160 is an FDA 510(k) premarket notification submitted by Misonix, Inc. for the device "neXus Ultrasonic Surgical Aspirator System". The FDA issued a decision of Substantially Equivalent on May 30, 2019. The device falls under product code LFL (Instrument, Ultrasonic Surgical), a Class U device. Misonix, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 30, 2019
Date Received
January 30, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Ultrasonic Surgical
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type