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Trackstar 302-WS380

by Veridian Healthcare

Trackstar 302-WS380 is a Class II device made by Veridian Healthcare, cleared under FDA 510(k) K233130 on 20 Dec 2023 and listed in FDA GUDID since 28 May 2026 (UDI-DI 00845717012171), active as of 24 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 24 Oct 2026

Documents

510(k) K233130

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845717012171 UDI-DI Date28 May 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberK233130 Date20 Dec 2023IssuedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K233130 decided 20 Dec 2023 Active
  • FDA GUDID UDI-DI 00845717012171 listed 28 May 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K233130
  2. Listed FDA GUDID 00845717012171

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Trackstar
Generic name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Model / reference
302-WS380
Primary DI / UDI-DI
00845717012171
510(k) Number
FDA product code
DXN
GMDN term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive).

Other devices from Veridian Healthcare

See all devices from Veridian Healthcare →

Properties

  • Over-the-counter
  • Lot / batch number
  • Serial number
Other properties (12, all answered No)