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Xltek 1411546

by Embla Systems

Xltek 1411546 is a Class II device made by Embla Systems, cleared under FDA 510(k) K024322 on 27 Oct 2003 and listed in FDA GUDID since 25 Oct 2016 (UDI-DI 00382830025393), 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) K024322

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 Number00382830025393 UDI-DI Date25 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK024322 Date27 Oct 2003DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K024322 decided 27 Oct 2003 Active
  • FDA GUDID UDI-DI 00382830025393 listed 25 Oct 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K024322
  2. Listed FDA GUDID 00382830025393

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Xltek
Generic name
Polysomnograph
Model / reference
1411546
Primary DI / UDI-DI
00382830025393
510(k) Number
FDA product code
MNR
GMDN term
Polysomnograph
Device class
Class II
Regulation number
868.2375
GUDID distribution status
In Commercial Distribution

Related devices

Category: Polysomnograph

Cleared under the same submission (K024322)

Similar devices in this category

Other devices filed under Polysomnograph.

Other devices from Embla Systems

See all devices from Embla Systems →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)