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Richmar 400-852

by Clearlake-Tech Inc.

Richmar 400-852 is a Class II device made by Clearlake-Tech Inc., listed in FDA GUDID since 2 Aug 2023 (UDI-DI 00850030915382), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850030915382 UDI-DI Date2 Aug 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Richmar
Generic name
Transcutaneous electrical stimulation electrode, reusable
Model / reference
400-852
Primary DI / UDI-DI
00850030915382
FDA product code
GXY
GMDN term
Transcutaneous electrical stimulation electrode, reusable
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution

Related devices

Category: Transcutaneous electrical stimulation electrode, reusable

Other devices from Clearlake-Tech Inc.

See all devices from Clearlake-Tech Inc. →

Properties

  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (12, all answered No)