510(k) K981527

MENTOR PATHWAY INTRODUCER/DILATOR by Mentor Corp. — Product Code QPB

K981527 is an FDA 510(k) premarket notification submitted by Mentor Corp. for the device "MENTOR PATHWAY INTRODUCER/DILATOR". The FDA issued a decision of Substantially Equivalent on July 9, 1998. The device falls under product code QPB (System, Suction, Lipoplasty For Removal), a Class II device regulated under 21 CFR 878.5040. Mentor Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 9, 1998
Date Received
April 28, 1998
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