510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K150134Substantially Equivalent

Basic, Dominant Flex, KV-6

Medela AG, Baar, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K150134 is the FDA 510(k) clearance record for Basic, Dominant Flex, KV-6, a class II device, cleared for Medela AG on under FDA product code QPB (System, Suction, Lipoplasty For Removal). FDA's definition for product code QPB reads: "A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring". FDA records list 56 510(k) clearances for Medela AG, from to . As of , FDA records show no recalls naming K150134.

Clearance record

Decision date
Received
(90 days to decision)
Product code
QPB System, Suction, Lipoplasty For Removal
Regulation
21 CFR 878.5040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Medela AG Lattichstrasse 4b, Baar, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QPB

Trailing 12 months
5 clearances under product code QPB in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QPB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20261
June 20261
July 20260
August 20261
September 20261
October 20260