Guangzhou Xinbo Electronic Co., Ltd.
Guangzhou Xinbo Electronic Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2024.
Top product codes for Guangzhou Xinbo Electronic Co., Ltd.
Recent clearances by Guangzhou Xinbo Electronic Co., Ltd.
- K230711 — Pain Therapy Device(Model: P.T.S-X)
- K231789 — Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)
- K231164 — Conductive carbon film electrode
- K231167 — Conductive Silicone Rubber Electrode
- K202671 — DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)
- K212948 — Pain Therapy Device(Model: DH-P.T.S-I, DH-P.T.S-II, DH-P.T.S-IIA, DH-P.T.S-IIB, DH-CP-I)
- K202636 — Metallic Fabric Electrodes
- K202638 — Pain Therapy Device
- K200402 — DR-HO'S Electro Therapy Conductive Gel
- K190118 — Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)
- K172887 — XinBo Electrode (Model: Neck Therapy Pro - I, Neck Therapy Pro - II, Neck Therapy Pro - III, Neck Therapy Pro - IV)
- K163611 — Pain Therapy Device
Data sourced from openFDA. This site is unofficial and independent of the FDA.