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MD Resource RM2000

by Medical Device Resource Corp.

MD Resource RM2000 is a Class II device made by Medical Device Resource Corp., cleared under FDA 510(k) K850704 on 24 May 1985 and listed in FDA GUDID since 13 Sep 2016 (UDI-DI 00859898006454), 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) K850704

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 Number00859898006454 UDI-DI Date13 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK850704 Date24 May 1985DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K850704 decided 24 May 1985 Active
  • FDA GUDID UDI-DI 00859898006454 listed 13 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K850704
  2. Listed FDA GUDID 00859898006454

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  • Withdrawn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
Surgical suction system
Model / Ref / Catalog
RM2000
Primary DI / UDI-DI
00859898006454
510(k) Number
FDA product code
JCX
GMDN term
Surgical suction system
Device class
Class II
Regulation number
878.4780
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered).

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)