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MD Resource LS2-DLS

by Medical Device Resource Corp.

MD Resource LS2-DLS is a Class II device made by Medical Device Resource Corp., cleared under FDA 510(k) K081593 on 23 Jul 2008 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00859898006379), active as of 22 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 22 Oct 2026

Documents

510(k) K081593

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00859898006379 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK081593 Date23 Jul 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K081593 decided 23 Jul 2008 Active
  • FDA GUDID UDI-DI 00859898006379 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K081593
  2. Listed FDA GUDID 00859898006379

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
MD Resource
Generic name
Liposuction system
Model / Ref / Catalog
LS2-DLS
Primary DI / UDI-DI
00859898006379
510(k) Number
FDA product code
MUU
GMDN term
Liposuction system
Device class
Class II
Regulation number
878.5040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Liposuction system

Cleared under the same submission (K081593)

Similar devices in this category

Other devices filed under Liposuction system.

Other devices from Medical Device Resource Corp.

See all devices from Medical Device Resource Corp. →

Properties

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