Pain Therapy Device(Model: P.T.S-X)— 510(k) K230711
Substantially EquivalentGuangzhou Xinbo Electronic Co., Ltd.
FDA 510(k) clearance K230711 for Pain Therapy Device(Model: P.T.S-X), Substantially Equivalent on 2024-05-16. Applicant: Guangzhou Xinbo Electronic Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd.
- Product code
- Code NGX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
Recent devices under product code NGX
view allMore clearances from Guangzhou Xinbo Electronic Co., Ltd.
view all- 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)
Data sourced from openFDA. This site is unofficial and independent of the FDA.