510(k) K012028

ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-5 by Misonix, Inc. — Product Code LFL

K012028 is an FDA 510(k) premarket notification submitted by Misonix, Inc. for the device "ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-5". The FDA issued a decision of Substantially Equivalent on July 27, 2001. 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
July 27, 2001
Date Received
June 28, 2001
Clearance Type
Special
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