FDA 510(k)

LAP-Pump PP110

K-Number: K163320 · 2017-03-21

Decision Date2017-03-21

Product CodeHET

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

LAP-Pump PP110 is a medical device manufactured by W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 2017-03-21 under approval number K163320. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAP-Pump PP110?

LAP-Pump PP110 is a medical device that received FDA 510(k) clearance on 2017-03-21. It is manufactured by W.O.M. World of Medicine GmbH. The 510(k) number is K163320.

When was LAP-Pump PP110 approved by the FDA?

LAP-Pump PP110 received FDA 510(k) clearance on 2017-03-21, under approval number K163320.

What company makes LAP-Pump PP110?

LAP-Pump PP110 is manufactured by W.O.M. World of Medicine GmbH.

What is the FDA product code for LAP-Pump PP110?

The FDA product code for LAP-Pump PP110 is HET.

Other Devices by W.O.M. World of Medicine GmbH

K153513Insufflator 50L FM134 K170784PNEUMOCLEAR K173311ARTHRO-Pump PA304 K173489GYN-Pump PH304 K172040Aquilex Fluid Control System AQL-100S K201361PNEUMOCLEAR

View all 8 devices →

Related Devices (Code: HET)

K173111LAP-iX Suction IrrigationSejong Medical Co., Ltd. K172796Flex Robotic System and Flex Transabdominal DriveMedrobotics Corporation K190190WV1 Endoscope270surgical , Ltd. K190744ENDOEYE HD II (WA50040A, WA50042A, WA50050A, WA50052A)Olympus Winter & Ibe GmbH K2002164K UHD Camera SystemScivita Medical Technology Co., Ltd. K200638LAP-iX Suction IrrigationSejong Medical Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.