Skip to content

Member's Mark 990513055

by Walmart Stores

Member's Mark 990513055 is a Class II device made by Walmart Stores, cleared under FDA 510(k) K244000 on 30 Apr 2025 and listed in FDA GUDID since 18 Feb 2026 (UDI-DI 00193968604929), 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) K244000

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 Number00193968604929 UDI-DI Date18 Feb 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) from GUDID NumberK244000 Date30 Apr 2025IssuedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K244000 decided 30 Apr 2025 Active
  • FDA GUDID UDI-DI 00193968604929 listed 18 Feb 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K244000
  2. Listed FDA GUDID 00193968604929

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Member's Mark
Generic name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Model / reference
990513055
Primary DI / UDI-DI
00193968604929
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
MRI safety
MR Unsafe

Similar devices

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

Other devices from Walmart Stores

See all devices from Walmart Stores →

Properties

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