510(k) K062471

ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RF by Misonix, Inc. — Product Code LFL

K062471 is an FDA 510(k) premarket notification submitted by Misonix, Inc. for the device "ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL FS 1000 RF". The FDA issued a decision of Substantially Equivalent on October 26, 2006. 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 26, 2006
Date Received
August 24, 2006
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