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Cathay CM6090FB

by Cathay Manufacturing Corp.

Cathay CM6090FB is a Class II device made by Cathay Manufacturing Corp., cleared under FDA 510(k) K020735 on 12 Jul 2002, registered in EUDAMED and listed in FDA GUDID since 17 Apr 2017 (UDI-DI 06959006302332), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K020735

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06959006302332 UDI-DI Date17 Apr 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK020735 Date12 Jul 2002DecidedStatusActive
European UnionCE/MDR EUDAMED Number— Date—StatusActive

Official records

Across registries

3 registries list this device

  • FDA 510(k) K020735 decided 12 Jul 2002 Active
  • EUDAMED Active
  • FDA GUDID UDI-DI 06959006302332 listed 17 Apr 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K020735
  2. Listed FDA GUDID 06959006302332

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Cathay
Generic name
Transcutaneous electrical stimulation electrode, single-use
Model / reference
CM6090FB
Primary DI / UDI-DI
06959006302332
510(k) Number
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution

Related devices

Category: Transcutaneous electrical stimulation electrode, single-use

Cleared under the same submission (K020735)

and 4 more cleared under K020735

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

Other devices from Cathay Manfacturing Corp.

See all devices from Cathay Manfacturing Corp. →

Properties

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