510(k) K000927

ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-4 by Misonix, Inc. — Product Code LFL

K000927 is an FDA 510(k) premarket notification submitted by Misonix, Inc. for the device "ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-4". The FDA issued a decision of Substantially Equivalent on October 10, 2000. 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
October 10, 2000
Date Received
March 22, 2000
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