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LAP-Pump PP120

by W.O.M. World of Medicine GmbH

LAP-Pump PP120 is a Class II device made by W.O.M. World of Medicine GmbH, cleared under FDA 510(k) K163320 on 21 Mar 2017 and listed in FDA GUDID since 27 Mar 2018 (UDI-DI 04056702001254), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K163320

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04056702001254 UDI-DI Date27 Mar 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK163320 Date21 Mar 2017DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K163320 decided 21 Mar 2017 Active
  • FDA GUDID UDI-DI 04056702001254 listed 27 Mar 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K163320
  2. Listed FDA GUDID 04056702001254

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
LAP-Pump
Generic name
Endoscopic irrigation/aspiration pump
Model / reference
PP120
Primary DI / UDI-DI
04056702001254
510(k) Number
FDA product code
HET
GMDN term
Endoscopic irrigation/aspiration pump
Device class
Class II
Regulation number
884.1720
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HET (Laparoscope, Gynecologic (And Accessories)).

Other devices from W.O.M. World of Medicine GmbH

See all devices from W.O.M. World of Medicine GmbH →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)