Moller Medical GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Moller Medical GmbH has 3 FDA 510(k) cleared medical devices. Based in Corona, US.
Historical record: 3 cleared submissions from 2013 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Moller Medical GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Moller Medical GmbH
3 devices
Cleared
Jun 19, 2017
Möller Medical Biopsy Needles and Systems
Gastroenterology & Urology
276d
Cleared
Dec 18, 2015
LiquoGuard 7, LiquoGuard 7 Drainage Set, Lenght 2000mm
Neurology
260d
Cleared
Dec 13, 2013
LIQUOGUARD CSF LIQUOGUARD CSF TUBING SET (1500MM) LIQUOGUARD CSF TUBING SET...
Neurology
597d