Skip to content

Sterile Hypodermic Needles for Single Use

by Zhejiang Kangkang Medical-Devices Co., Ltd. 510(k)

Active United States

510(k) K210232

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK210232 Date23 Sep 2021ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
FMI
Device Class
Class II
Regulation
21 CFR Part 880.5570
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Other devices from Zhejiang Kangkang Medical-Devices Co., Ltd.

See all devices from Zhejiang Kangkang Medical-Devices Co., Ltd. →