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Scian Ld-737S

by Honsun (Nantong) Co., Ltd 2 variants

Scian Ld-737S 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 31 Mar 2022 (UDI-DI 16970384250647), 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) K131463

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 Number16970384250647 UDI-DI Date31 Mar 2022ListedStatusListed 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 16970384250647 listed 31 Mar 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131463
  2. Listed FDA GUDID 16970384250647

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Scian
Generic name
Automatic-inflation electronic sphygmomanometer, portable, finger
Model / reference
LD-737S
Primary DI / UDI-DI
16970384250647
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

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
Other properties (14, all answered No)