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)

IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D

K-Number: K092763 · 2009-10-08

ApplicantWell-Life Healthcare Limited
Decision Date2009-10-08
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D is the device name listed in this FDA 510(k) record. The listed applicant is Well-Life Healthcare Limited. It received FDA 510(k) clearance on 2009-10-08 under 510(k) number K092763. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D?

IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D is a medical device that received FDA 510(k) clearance on 2009-10-08. The listed applicant is Well-Life Healthcare Limited. The 510(k) number is K092763.

When did IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D receive FDA 510(k) clearance?

IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D received FDA 510(k) clearance on 2009-10-08, under 510(k) number K092763.

Who is the listed applicant for IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D?

The FDA 510(k) record lists Well-Life Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D?

The FDA product code for IF TRUE SINE INTERFERENTIAL STIMULATOR, WL-2206D is LIH.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Well-Life Healthcare Limited as applicant

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.

K233054Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus StimulatorK222528Well-Life Probe Electrode for Stimulation/EMG Probe (Model: SA), Well-Life Incontinence Stimulation/EMG Electrode Probe, Well-Life Probe ElectrodeK220524Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)K213091Well-Life TENS/EMS/Heating StimulatorK200942Well-Life Garment Electrodes (GM Series)K172809OTC Combo TENS/EMS System

View all 20 devices →

Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments 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.

↑