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Lccs ET1690-Lc

by Lccs Products Limited

Lccs ET1690-Lc is a Class II device made by Lccs Products Limited, cleared under FDA 510(k) K131006 on 6 Dec 2013 and listed in FDA GUDID since 24 Jul 2021 (UDI-DI 04895233608415), 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) K131006

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 Number04895233608415 UDI-DI Date24 Jul 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK131006 Date6 Dec 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131006 decided 6 Dec 2013 Active
  • FDA GUDID UDI-DI 04895233608415 listed 24 Jul 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131006
  2. Listed FDA GUDID 04895233608415

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Lccs
Generic name
Epidural needle, non-threaded
Model / reference
ET1690-LC
Primary DI / UDI-DI
04895233608415
510(k) Number
FDA product code
BSP
GMDN term
Epidural needle, non-threaded
Device class
Class II
Regulation number
868.5150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)).

Other devices from Lccs Products Limited

See all devices from Lccs Products Limited →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)