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Welby LD-753

by Honsun (Nantong) Co., Ltd 2 variants

Welby LD-753 is a Class II device made by Honsun (Nantong) Co., Ltd, cleared under FDA 510(k) K131463 on 8 Jul 2013 and listed in FDA GUDID since 3 Feb 2018 (UDI-DI 00697038425624), active as of 22 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 22 Oct 2026

Documents

510(k) K131463

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00697038425624 UDI-DI Date3 Feb 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK131463 Date8 Jul 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131463 decided 8 Jul 2013 Active
  • FDA GUDID UDI-DI 00697038425624 listed 3 Feb 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131463
  2. Listed FDA GUDID 00697038425624

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Welby
Generic name
Automatic-inflation electronic sphygmomanometer, portable, finger
Model / reference
LD-753
Primary DI / UDI-DI
00697038425624
510(k) Number
FDA product code
DXN
GMDN term
Automatic-inflation electronic sphygmomanometer, portable, finger
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Similar devices

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

Other devices from Honsun (Nantong) Co., Ltd

See all devices from Honsun (Nantong) Co., Ltd →

Properties

  • Lot / batch number
  • Serial number
Other properties (13, all answered No)