510(k) K992282

MICRO-FRANCE LIPOSUCTION CANNULAS by Xomed, Inc. — Product Code QPB

K992282 is an FDA 510(k) premarket notification submitted by Xomed, Inc. for the device "MICRO-FRANCE LIPOSUCTION CANNULAS". The FDA issued a decision of Substantially Equivalent on September 23, 1999. The device falls under product code QPB (System, Suction, Lipoplasty For Removal), a Class II device regulated under 21 CFR 878.5040. Xomed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 23, 1999
Date Received
July 7, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Suction, Lipoplasty For Removal
Device Class
Class II
Regulation Number
878.5040
Review Panel
SU
Submission Type

A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring