Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ELECTRODES PAD

K-Number: K190700 · 2019-06-14

ApplicantShenzhen Bestpad Technology Development Co., Ltd.
Decision Date2019-06-14
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRODES PAD is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Bestpad Technology Development Co., Ltd.. It received FDA 510(k) clearance on 2019-06-14 under 510(k) number K190700. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODES PAD?

ELECTRODES PAD is a medical device that received FDA 510(k) clearance on 2019-06-14. The listed applicant is Shenzhen Bestpad Technology Development Co., Ltd.. The 510(k) number is K190700.

When did ELECTRODES PAD receive FDA 510(k) clearance?

ELECTRODES PAD received FDA 510(k) clearance on 2019-06-14, under 510(k) number K190700.

Who is the listed applicant for ELECTRODES PAD?

The FDA 510(k) record lists Shenzhen Bestpad Technology Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRODES PAD?

The FDA product code for ELECTRODES PAD is GXY.

Related Devices (Code: GXY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260578Ambu® NeurolineTM Cup MRI/CT (Models 72704/21US, 72704/23US, 72704/25US, 72704/27US) Ambu® NeurolineTM Cup MRI/CT-set (Models 72704/21-1010US, 72704/21-1010US, 72704/23-1010US, 72704/25-1010US, 72704/27-1010US) Ambu® NeurolineTM Cup MRI/CT-mini set (Models 72704/21-0301US, 72704/23-0301US, 72704/25-0301US, 72704/27-0301US)Ambu A/SK261442Charlotte ACC25 Surface Electrode Array; Charlotte ACC25 Reusable Surface Electrode ArrayCadwell Industries, Inc.K261522BioWave BioWrapsBiowave CorporationK253237Elde Medical Electrodes (T5/ 5 cm x 5cm electrode T10/ 5 cm x 10cm electrode)Elde Medikal Sanayi ve Ticaret Anonim SirketiK254183MR Conditional Cup ElectrodesTechnomed EuropeK252439Tutamen Self Adhesive ElectrodesDongguan Tutamen Metalwork Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑