Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K150898Substantially Equivalent

LiquoGuard 7, LiquoGuard 7 Drainage Set, Lenght 2000mm

Moller Medical GmbH, Fulda, DE / Traditional, Substantially Equivalent

K150898 is the FDA 510(k) clearance record for LiquoGuard 7, LiquoGuard 7 Drainage Set, Lenght 2000mm, a class II device, cleared for Moller Medical GmbH on under FDA product code JXG (Shunt, Central Nervous System And Components). FDA records list 3 510(k) clearances for Moller Medical GmbH, from to . As of , FDA records show no recalls naming K150898.

Clearance record

Decision date
Received
(260 days to decision)
Product code
JXG Shunt, Central Nervous System And Components
Regulation
21 CFR 882.5550
Device class
Class II
Review panel
Neurology
Applicant
Moller Medical GmbH Wasserkuppenstr.29-31, Fulda, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JXG

Trailing 12 months
5 clearances under product code JXG in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JXG, trailing twelve months
MonthClearances
November 20252
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20261